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rs397507815

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397507815(-;-)
Make rs397507815(-;CT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340309
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507815
ebirs397507815
HLIrs397507815
Exacrs397507815
Varsomers397507815
Maprs397507815
PheGenIrs397507815
hapmaprs397507815
1000 genomesrs397507815
hgdprs397507815
ensemblrs397507815
gopubmedrs397507815
geneviewrs397507815
scholarrs397507815
googlers397507815
pharmgkbrs397507815
gwascentralrs397507815
openSNPrs397507815
23andMers397507815
23andMe allrs397507815
SNP Nexus

SNPshotrs397507815
SNPdbers397507815
MSV3drs397507815
GWAS Ctlgrs397507815
Max Magnitude0
ClinVar
Risk rs397507815(;)
Alt rs397507815(;)
Reference rs397507815(TC;TC)
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.32914446_32914447delCT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044802.2, RCV000113509.1,