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rs397508000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508000(A;T)
Make rs397508000(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376681
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508000
ebirs397508000
HLIrs397508000
Exacrs397508000
Varsomers397508000
Maprs397508000
PheGenIrs397508000
hapmaprs397508000
1000 genomesrs397508000
hgdprs397508000
ensemblrs397508000
gopubmedrs397508000
geneviewrs397508000
scholarrs397508000
googlers397508000
pharmgkbrs397508000
gwascentralrs397508000
openSNPrs397508000
23andMers397508000
23andMe allrs397508000
SNP Nexus

SNPshotrs397508000
SNPdbers397508000
MSV3drs397508000
GWAS Ctlgrs397508000
Max Magnitude0
ClinVar
Risk rs397508000(T;T)
Alt rs397508000(T;T)
Reference rs397508000(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32950818A>T
CLNSRC ClinVar
CLNACC RCV000045588.2,