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rs397507371

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATAATCAC;ATAATCAC) 0 common in clinvar
Make rs397507371(-;-)
Make rs397507371(-;ATAATCAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340789
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507371
ebirs397507371
HLIrs397507371
Exacrs397507371
Varsomers397507371
Maprs397507371
PheGenIrs397507371
hapmaprs397507371
1000 genomesrs397507371
hgdprs397507371
ensemblrs397507371
gopubmedrs397507371
geneviewrs397507371
scholarrs397507371
googlers397507371
pharmgkbrs397507371
gwascentralrs397507371
openSNPrs397507371
23andMers397507371
23andMe allrs397507371
SNP Nexus

SNPshotrs397507371
SNPdbers397507371
MSV3drs397507371
GWAS Ctlgrs397507371
Max Magnitude0
ClinVar
Risk rs397507371(;)
Alt rs397507371(;)
Reference rs397507371(ATAATCAC;ATAATCAC)
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.32914926_32914933delATAATCAC
CLNSRC ClinVar
CLNACC RCV000031626.3, RCV000044946.2,