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rs397508062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATGCATATACTGCA;ATGCATATACTGCA) 0 common in clinvar
Make rs397508062(-;-)
Make rs397508062(-;ATGCATATACTGCA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32396937
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508062
ebirs397508062
HLIrs397508062
Exacrs397508062
Varsomers397508062
Maprs397508062
PheGenIrs397508062
hapmaprs397508062
1000 genomesrs397508062
hgdprs397508062
ensemblrs397508062
gopubmedrs397508062
geneviewrs397508062
scholarrs397508062
googlers397508062
pharmgkbrs397508062
gwascentralrs397508062
openSNPrs397508062
23andMers397508062
23andMe allrs397508062
SNP Nexus

SNPshotrs397508062
SNPdbers397508062
MSV3drs397508062
GWAS Ctlgrs397508062
Max Magnitude0
ClinVar
Risk rs397508062(;)
Alt rs397508062(;)
Reference rs397508062(ATGCATATACTGCA;ATGCATATACTGCA)
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.32971074_32971087delATGCATATACTGCA
CLNSRC ClinVar
CLNACC RCV000045852.2, RCV000077473.2,