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rs397507386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507386(-;-)
Make rs397507386(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355195
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507386
ebirs397507386
HLIrs397507386
Exacrs397507386
Varsomers397507386
Maprs397507386
PheGenIrs397507386
hapmaprs397507386
1000 genomesrs397507386
hgdprs397507386
ensemblrs397507386
gopubmedrs397507386
geneviewrs397507386
scholarrs397507386
googlers397507386
pharmgkbrs397507386
gwascentralrs397507386
openSNPrs397507386
23andMers397507386
23andMe allrs397507386
SNP Nexus

SNPshotrs397507386
SNPdbers397507386
MSV3drs397507386
GWAS Ctlgrs397507386
Max Magnitude0
ClinVar
Risk rs397507386(;)
Alt rs397507386(;)
Reference rs397507386(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.32929332_32929333delAA
CLNSRC ClinVar
CLNACC RCV000031672.3,