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rs397507666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507666(-;-)
Make rs397507666(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337736
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507666
ebirs397507666
HLIrs397507666
Exacrs397507666
Varsomers397507666
Maprs397507666
PheGenIrs397507666
hapmaprs397507666
1000 genomesrs397507666
hgdprs397507666
ensemblrs397507666
gopubmedrs397507666
geneviewrs397507666
scholarrs397507666
googlers397507666
pharmgkbrs397507666
gwascentralrs397507666
openSNPrs397507666
23andMers397507666
23andMe allrs397507666
SNP Nexus

SNPshotrs397507666
SNPdbers397507666
MSV3drs397507666
GWAS Ctlgrs397507666
Max Magnitude0
ClinVar
Risk rs397507666(;)
Alt rs397507666(;)
Reference rs397507666(T;T)
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.32911873delT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044184.2, RCV000113167.1,