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rs397508038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508038(A;A)
Make rs397508038(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379915
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508038
ebirs397508038
HLIrs397508038
Exacrs397508038
Varsomers397508038
Maprs397508038
PheGenIrs397508038
hapmaprs397508038
1000 genomesrs397508038
hgdprs397508038
ensemblrs397508038
gopubmedrs397508038
geneviewrs397508038
scholarrs397508038
googlers397508038
pharmgkbrs397508038
gwascentralrs397508038
openSNPrs397508038
23andMers397508038
23andMe allrs397508038
SNP Nexus

SNPshotrs397508038
SNPdbers397508038
MSV3drs397508038
GWAS Ctlgrs397508038
Max Magnitude0
ClinVar
Risk rs397508038(A;A)
Alt rs397508038(A;A)
Reference rs397508038(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32954052T>A
CLNSRC ClinVar
CLNACC RCV000045723.2,