Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs397507285(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336781
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507285
ebirs397507285
HLIrs397507285
Exacrs397507285
Varsomers397507285
Maprs397507285
PheGenIrs397507285
hapmaprs397507285
1000 genomesrs397507285
hgdprs397507285
ensemblrs397507285
gopubmedrs397507285
geneviewrs397507285
scholarrs397507285
googlers397507285
pharmgkbrs397507285
gwascentralrs397507285
openSNPrs397507285
23andMers397507285
23andMe allrs397507285
SNP Nexus

SNPshotrs397507285
SNPdbers397507285
MSV3drs397507285
GWAS Ctlgrs397507285
Max Magnitude6
ClinVar
Risk rs397507285(G;G)
Alt rs397507285(G;G)
Reference rs397507285(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32910918T>G
CLNSRC ClinVar
CLNACC RCV000031367.3, RCV000160047.2, RCV000204854.1,