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rs397507609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507609(-;-)
Make rs397507609(-;A)
Make rs397507609(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333293
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507609
ebirs397507609
HLIrs397507609
Exacrs397507609
Varsomers397507609
Maprs397507609
PheGenIrs397507609
hapmaprs397507609
1000 genomesrs397507609
hgdprs397507609
ensemblrs397507609
gopubmedrs397507609
geneviewrs397507609
scholarrs397507609
googlers397507609
pharmgkbrs397507609
gwascentralrs397507609
openSNPrs397507609
23andMers397507609
23andMe allrs397507609
SNP Nexus

SNPshotrs397507609
SNPdbers397507609
MSV3drs397507609
GWAS Ctlgrs397507609
Max Magnitude0
ClinVar
Risk rs397507609(A;A)
Alt rs397507609(A;A)
Reference rs397507609(;)
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.32907430dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000043898.2, RCV000112980.1,