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rs397507406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGG;AAGG) 0 common in clinvar
(GAAG;GAAG) 0 common in clinvar
Make rs397507406(-;-)
Make rs397507406(-;GAAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371016
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507406
ebirs397507406
HLIrs397507406
Exacrs397507406
Varsomers397507406
Maprs397507406
PheGenIrs397507406
hapmaprs397507406
1000 genomesrs397507406
hgdprs397507406
ensemblrs397507406
gopubmedrs397507406
geneviewrs397507406
scholarrs397507406
googlers397507406
pharmgkbrs397507406
gwascentralrs397507406
openSNPrs397507406
23andMers397507406
23andMe allrs397507406
SNP Nexus

SNPshotrs397507406
SNPdbers397507406
MSV3drs397507406
GWAS Ctlgrs397507406
Max Magnitude0
ClinVar
Risk rs397507406(;)
Alt rs397507406(;)
Reference rs397507406(AAGG;AAGG)
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.32945153_32945156delGAAG
CLNSRC ClinVar
CLNACC RCV000031750.3, RCV000045555.2,