RGD:8697607 Rat Genome Database

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Variant: RGD:8697607 -  Homo sapiens

RGD ID: 8697607
RS ID: rs587782167
ClinVar ID: CV151710
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 37,034,760
GRCh38 3 36,993,269
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_216t1:c.-279A>G
LRG_216:g.4920A>G
NG_007109.2:g.4920A>G
NC_000003.12:g.36993269A>G
More... 		02/21/2019 2kb upstream variant|upstream transcript variant 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 RCV000130761 CLINVAR
dbSNP (RS) rs587782167 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene MLH1 CLINVAR
OMIM 120436 CLINVAR
SNOMED CT 699346009 CLINVAR