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rs397507779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
(AA;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507779(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339705
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507779
ClinGenrs397507779
ebirs397507779
HLIrs397507779
Exacrs397507779
Varsomers397507779
Maprs397507779
PheGenIrs397507779
hapmaprs397507779
1000 genomesrs397507779
hgdprs397507779
ensemblrs397507779
gopubmedrs397507779
geneviewrs397507779
scholarrs397507779
googlers397507779
pharmgkbrs397507779
gwascentralrs397507779
openSNPrs397507779
23andMers397507779
23andMe allrs397507779
SNP Nexus

SNPshotrs397507779
SNPdbers397507779
MSV3drs397507779
GWAS Ctlgrs397507779
Max Magnitude6
ClinVar
Risk rs397507779(T;T)
Alt rs397507779(T;T)
Reference Rs397507779(AA;AA)
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.32913842_32913843delAAinsT
CLNSRC ClinVar
CLNACC RCV000044640.2, RCV000256629.2,