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rs397507800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507800(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340089
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507800
dbSNP (old)rs397507800
ClinGenrs397507800
ebirs397507800
HLIrs397507800
Exacrs397507800
Gnomadrs397507800
Varsomers397507800
Maprs397507800
PheGenIrs397507800
Biobankrs397507800
1000 genomesrs397507800
hgdprs397507800
ensemblrs397507800
gopubmedrs397507800
geneviewrs397507800
scholarrs397507800
googlers397507800
pharmgkbrs397507800
gwascentralrs397507800
openSNPrs397507800
23andMers397507800
23andMe allrs397507800
SNP Nexus

SNPshotrs397507800
SNPdbers397507800
MSV3drs397507800
GWAS Ctlgrs397507800
Max Magnitude6
ClinVar
Risk rs397507800(T;T)
Alt rs397507800(T;T)
Reference Rs397507800(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914226G>T
CLNSRC ClinVar
CLNACC RCV000044737.2, RCV000257767.2,