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rs397507328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507328(-;-)
Make rs397507328(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338674
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507328
ebirs397507328
HLIrs397507328
Exacrs397507328
Varsomers397507328
Maprs397507328
PheGenIrs397507328
hapmaprs397507328
1000 genomesrs397507328
hgdprs397507328
ensemblrs397507328
gopubmedrs397507328
geneviewrs397507328
scholarrs397507328
googlers397507328
pharmgkbrs397507328
gwascentralrs397507328
openSNPrs397507328
23andMers397507328
23andMe allrs397507328
SNP Nexus

SNPshotrs397507328
SNPdbers397507328
MSV3drs397507328
GWAS Ctlgrs397507328
Max Magnitude0
ClinVar
Risk rs397507328(;)
Alt rs397507328(;)
Reference rs397507328(AA;AA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912811_32912812delAA
CLNSRC ClinVar
CLNACC RCV000031475.3,