RGD:25327936 Rat Genome Database

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Variant: RGD:25327936 -  Homo sapiens

RGD ID: 25327936
RS ID: rs1575373603
ClinVar ID: CV815290
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 37,034,820
GRCh38 3 36,993,329
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_216t1:c.-219G>T
LRG_216:g.4980G>T
NG_008418.1:g.4976C>A
NG_007109.2:g.4980G>T
More...
07/12/2019 uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001014766 CLINVAR
dbSNP (RS) rs1575373603 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene MLH1 CLINVAR
OMIM 120436 CLINVAR
SNOMED CT 699346009 CLINVAR