| 156400881 | CV2217362 | single nucleotide variant | NM_080753.3(WFDC10A):c.13A>G (p.Thr5Ala) | Inborn genetic diseases [RCV002656719] | likely benign | 20 | 45629826 | 45629826 | Human | 1 | name |
| 156267294 | CV2329665 | single nucleotide variant | NM_080753.3(WFDC10A):c.78G>C (p.Lys26Asn) | not specified [RCV004180777] | uncertain significance | 20 | 45629891 | 45629891 | Human | | name |
| 329360570 | CV2439508 | single nucleotide variant | NM_080753.3(WFDC10A):c.73G>A (p.Asp25Asn) | not specified [RCV004262447] | uncertain significance | 20 | 45629886 | 45629886 | Human | | name |
| 329401084 | CV2446098 | single nucleotide variant | NM_080753.3(WFDC10A):c.81G>C (p.Lys27Asn) | not specified [RCV004270654] | uncertain significance | 20 | 45629894 | 45629894 | Human | | name |
| 401758752 | CV2705110 | single nucleotide variant | NM_080753.3(WFDC10A):c.55G>T (p.Ala19Ser) | not specified [RCV004310014] | uncertain significance | 20 | 45629868 | 45629868 | Human | | name |
| 156326516 | CV2205780 | single nucleotide variant | NM_080753.3(WFDC10A):c.185C>A (p.Ala62Glu) | not specified [RCV004599443] | uncertain significance | 20 | 45630963 | 45630963 | Human | | name |
| 155976255 | CV2266277 | single nucleotide variant | NM_080753.3(WFDC10A):c.193A>G (p.Ile65Val) | not specified [RCV004129110] | uncertain significance | 20 | 45630971 | 45630971 | Human | | name |
| 329352429 | CV2453009 | single nucleotide variant | NM_080753.3(WFDC10A):c.155A>T (p.His52Leu) | not specified [RCV004277629] | uncertain significance | 20 | 45630933 | 45630933 | Human | | name |
| 405807809 | CV3356632 | single nucleotide variant | NM_080753.3(WFDC10A):c.119T>A (p.Val40Asp) | not specified [RCV004480892] | uncertain significance | 20 | 45630897 | 45630897 | Human | | name |
| 407487896 | CV3490021 | single nucleotide variant | NM_080753.3(WFDC10A):c.117A>C (p.Lys39Asn) | not specified [RCV004678436] | uncertain significance | 20 | 45630895 | 45630895 | Human | | name |
| 597792217 | CV3630182 | single nucleotide variant | NM_080753.3(WFDC10A):c.199T>C (p.Cys67Arg) | not specified [RCV004876920] | uncertain significance | 20 | 45630977 | 45630977 | Human | | name |