RGD:11093902 Rat Genome Database

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Variant: RGD:11093902 -  Homo sapiens

RGD ID: 11093902
RS ID: rs876658668
ClinVar ID: CV232486
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 47,630,169
GRCh38 2 47,403,030
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
LRG_218:g.4907C>T
NG_007110.2:g.4907C>T
NC_000002.12:g.47403030C>T
NC_000002.11:g.47630169C>T
More... 		06/27/2019 2kb upstream variant|intron variant uncertain significance adult 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 RCV000220356 CLINVAR
dbSNP (RS) rs876658668 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene MSH2 CLINVAR
OMIM 609309 CLINVAR
SNOMED CT 699346009 CLINVAR