| 15123682 | CV708844 | single nucleotide variant | NM_001337.4(CX3CR1):c.117C>T (p.Ser39=) | not provided [RCV000963288] | likely benign | 3 | 39266393 | 39266393 | Human | | name |
| 405284775 | CV3190829 | single nucleotide variant | NM_001337.4(CX3CR1):c.657T>C (p.Phe219=) | CX3CR1-related disorder [RCV003909396] | likely benign | 3 | 39265853 | 39265853 | Human | | name , trait , alternate_id |
| 405275113 | CV3204381 | single nucleotide variant | NM_001171174.1(CX3CR1):c.21G>A (p.Ala7=) | CX3CR1-related disorder [RCV003934586] | likely benign | 3 | 39281675 | 39281675 | Human | | name , trait , alternate_id |
| 407473278 | CV3419955 | single nucleotide variant | NM_001337.4(CX3CR1):c.38A>G (p.Glu13Gly) | not specified [RCV004616178] | uncertain significance | 3 | 39266472 | 39266472 | Human | | name |
| 15202836 | CV698076 | single nucleotide variant | NM_001337.4(CX3CR1):c.74A>G (p.Asp25Gly) | CX3CR1-related disorder [RCV003903317]|not provided [RCV000958062] | likely benign | 3 | 39266436 | 39266436 | Human | | name , trait , alternate_id |
| 15184946 | CV698077 | single nucleotide variant | NM_001337.4(CX3CR1):c.39G>T (p.Glu13Asp) | not provided [RCV000952834] | benign | 3 | 39266471 | 39266471 | Human | | name |
| 15167226 | CV708843 | single nucleotide variant | NM_001337.4(CX3CR1):c.765G>A (p.Thr255=) | not provided [RCV000971356] | benign|likely benign | 3 | 39265745 | 39265745 | Human | | name |
| 15113756 | CV720433 | single nucleotide variant | NM_001337.4(CX3CR1):c.456C>T (p.Gly152=) | not provided [RCV000894726] | benign | 3 | 39266054 | 39266054 | Human | | name |
| 15114420 | CV734051 | single nucleotide variant | NM_001337.4(CX3CR1):c.576T>C (p.Asn192=) | not provided [RCV000894852] | likely benign | 3 | 39265934 | 39265934 | Human | | name |
| 15137801 | CV763886 | single nucleotide variant | NM_001337.4(CX3CR1):c.825C>T (p.Leu275=) | not provided [RCV000943297] | likely benign | 3 | 39265685 | 39265685 | Human | | name |
| 401730218 | CV2680048 | single nucleotide variant | NM_001337.4(CX3CR1):c.296A>G (p.Asn99Ser) | not specified [RCV004286544] | uncertain significance | 3 | 39266214 | 39266214 | Human | | name |
| 598236509 | CV3956145 | single nucleotide variant | NM_001337.4(CX3CR1):c.199G>A (p.Asp67Asn) | not specified [RCV005320447] | uncertain significance | 3 | 39266311 | 39266311 | Human | | name |
| 15203226 | CV698075 | single nucleotide variant | NM_001337.4(CX3CR1):c.169A>G (p.Thr57Ala) | not provided [RCV000958294] | likely benign | 3 | 39266341 | 39266341 | Human | | name |
| 15133191 | CV708842 | single nucleotide variant | NM_001337.4(CX3CR1):c.1054T>C (p.Leu352=) | not provided [RCV000964907] | benign | 3 | 39265456 | 39265456 | Human | | name |
| 126910039 | CV1037397 | single nucleotide variant | NM_001337.4(CX3CR1):c.319G>A (p.Ala107Thr) | not provided [RCV001354309] | uncertain significance | 3 | 39266191 | 39266191 | Human | | name |
| 8649281 | CV125774 | single nucleotide variant | NM_001337.4(CX3CR1):c.785T>C (p.Phe262Ser) | not provided [RCV000106289] | not provided | 3 | 39265725 | 39265725 | Human | | name |
| 156274576 | CV2202635 | single nucleotide variant | NM_001337.4(CX3CR1):c.356T>C (p.Phe119Ser) | not specified [RCV004082890] | uncertain significance | 3 | 39266154 | 39266154 | Human | | name |
| 156137169 | CV2253404 | single nucleotide variant | NM_001337.4(CX3CR1):c.547C>T (p.Leu183Phe) | not specified [RCV004125135] | uncertain significance | 3 | 39265963 | 39265963 | Human | | name |
| 155908831 | CV2307158 | single nucleotide variant | NM_001337.4(CX3CR1):c.850A>G (p.Ser284Gly) | not specified [RCV004159634] | uncertain significance | 3 | 39265660 | 39265660 | Human | | name |
| 156305767 | CV2314736 | single nucleotide variant | NM_001337.4(CX3CR1):c.732G>C (p.Trp244Cys) | not specified [RCV004170878] | uncertain significance | 3 | 39265778 | 39265778 | Human | | name |
| 156012689 | CV2358944 | single nucleotide variant | NM_001337.4(CX3CR1):c.979T>A (p.Ser327Thr) | not specified [RCV004212277] | uncertain significance | 3 | 39265531 | 39265531 | Human | | name |
| 156176448 | CV2374447 | single nucleotide variant | NM_001337.4(CX3CR1):c.565G>A (p.Val189Met) | not specified [RCV004231956] | uncertain significance | 3 | 39265945 | 39265945 | Human | | name |
| 156072993 | CV2376876 | single nucleotide variant | NM_001337.4(CX3CR1):c.952C>T (p.Arg318Cys) | not specified [RCV004229575] | uncertain significance | 3 | 39265558 | 39265558 | Human | | name |
| 329360588 | CV2439516 | single nucleotide variant | NM_001337.4(CX3CR1):c.772C>T (p.Leu258Phe) | not specified [RCV004262454] | uncertain significance | 3 | 39265738 | 39265738 | Human | | name |
| 401727326 | CV2684578 | single nucleotide variant | NM_001337.4(CX3CR1):c.734C>T (p.Thr245Ile) | not specified [RCV004293686] | uncertain significance | 3 | 39265776 | 39265776 | Human | | name |
| 401860420 | CV2762429 | single nucleotide variant | NM_001337.4(CX3CR1):c.832A>G (p.Thr278Ala) | not specified [RCV004335529] | uncertain significance | 3 | 39265678 | 39265678 | Human | | name |
| 401882170 | CV2774723 | single nucleotide variant | NM_001337.4(CX3CR1):c.485C>T (p.Ala162Val) | not specified [RCV004343825] | uncertain significance | 3 | 39266025 | 39266025 | Human | | name |
| 405262373 | CV3200172 | single nucleotide variant | NM_001337.4(CX3CR1):c.571C>T (p.Arg191Cys) | CX3CR1-related disorder [RCV003967277] | likely benign | 3 | 39265939 | 39265939 | Human | | name , trait , alternate_id |
| 405665437 | CV3243190 | single nucleotide variant | NM_001337.4(CX3CR1):c.376G>T (p.Asp126Tyr) | not specified [RCV004367543] | uncertain significance | 3 | 39266134 | 39266134 | Human | | name |
| 405665440 | CV3243191 | single nucleotide variant | NM_001337.4(CX3CR1):c.485C>G (p.Ala162Gly) | not specified [RCV004367544] | uncertain significance | 3 | 39266025 | 39266025 | Human | | name |
| 405665444 | CV3243192 | single nucleotide variant | NM_001337.4(CX3CR1):c.529G>A (p.Gly177Ser) | not specified [RCV004367545] | uncertain significance | 3 | 39265981 | 39265981 | Human | | name |
| 405665448 | CV3243193 | single nucleotide variant | NM_001337.4(CX3CR1):c.980C>T (p.Ser327Phe) | not specified [RCV004367546] | uncertain significance | 3 | 39265530 | 39265530 | Human | | name |
| 598236513 | CV3956146 | single nucleotide variant | NM_001337.4(CX3CR1):c.698T>C (p.Ile233Thr) | not specified [RCV005320448] | uncertain significance | 3 | 39265812 | 39265812 | Human | | name |
| 598160375 | CV3956147 | single nucleotide variant | NM_001337.4(CX3CR1):c.675G>T (p.Lys225Asn) | not specified [RCV005328759] | uncertain significance | 3 | 39265835 | 39265835 | Human | | name |
| 598236518 | CV3956148 | single nucleotide variant | NM_001337.4(CX3CR1):c.659C>T (p.Ser220Phe) | not specified [RCV005320449] | uncertain significance | 3 | 39265851 | 39265851 | Human | | name |
| 15169580 | CV748252 | single nucleotide variant | NM_001337.4(CX3CR1):c.335G>C (p.Gly112Ala) | not provided [RCV000927527] | likely benign | 3 | 39266175 | 39266175 | Human | | name |
| 41406564 | CV980451 | single nucleotide variant | NM_001171174.1(CX3CR1):c.10C>G (p.Pro4Ala) | CX3CR1-related disorder [RCV003918817]|Coronary heart disease, susceptibility to, 1 [RCV001280984]|not provided [RCV004692402] | benign|uncertain significance | 3 | 39281686 | 39281686 | Human | 3 | name , trait , alternate_id |
