RGD:155699976 Rat Genome Database

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Variant: RGD:155699976 -  Homo sapiens

RGD ID: 155699976
ClinVar ID: CV1791820
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 47,630,015
GRCh38 2 47,402,876
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000002.11:g.47630015G>C
LRG_218:g.4753G>C
NG_007110.2:g.4753G>C
NG_095167.1:g.80G>C
More... 		01/02/2020 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 RCV002322623 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene LOC129933695 CLINVAR
  MSH2 CLINVAR
OMIM 609309 CLINVAR
SNOMED CT 699346009 CLINVAR