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rs397507272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507272(-;-)
Make rs397507272(-;A)
Make rs397507272(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333071
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507272
ebirs397507272
HLIrs397507272
Exacrs397507272
Varsomers397507272
Maprs397507272
PheGenIrs397507272
hapmaprs397507272
1000 genomesrs397507272
hgdprs397507272
ensemblrs397507272
gopubmedrs397507272
geneviewrs397507272
scholarrs397507272
googlers397507272
pharmgkbrs397507272
gwascentralrs397507272
openSNPrs397507272
23andMers397507272
23andMe allrs397507272
SNP Nexus

SNPshotrs397507272
SNPdbers397507272
MSV3drs397507272
GWAS Ctlgrs397507272
Max Magnitude0
ClinVar
Risk rs397507272(A;A)
Alt rs397507272(A;A)
Reference rs397507272(;)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907208dupA
CLNSRC ClinVar
CLNACC RCV000031329.3, RCV000043834.2,