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rs397507726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507726(-;-)
Make rs397507726(-;A)
Make rs397507726(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338901
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507726
ebirs397507726
HLIrs397507726
Exacrs397507726
Varsomers397507726
Maprs397507726
PheGenIrs397507726
hapmaprs397507726
1000 genomesrs397507726
hgdprs397507726
ensemblrs397507726
gopubmedrs397507726
geneviewrs397507726
scholarrs397507726
googlers397507726
pharmgkbrs397507726
gwascentralrs397507726
openSNPrs397507726
23andMers397507726
23andMe allrs397507726
SNP Nexus

SNPshotrs397507726
SNPdbers397507726
MSV3drs397507726
GWAS Ctlgrs397507726
Max Magnitude0
ClinVar
Risk rs397507726(A;A)
Alt rs397507726(A;A)
Reference rs397507726(;)
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.32913038dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044435.2, RCV000113317.1,