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rs397508044

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508044(A;A)
Make rs397508044(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394723
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508044
ebirs397508044
HLIrs397508044
Exacrs397508044
Varsomers397508044
Maprs397508044
PheGenIrs397508044
hapmaprs397508044
1000 genomesrs397508044
hgdprs397508044
ensemblrs397508044
gopubmedrs397508044
geneviewrs397508044
scholarrs397508044
googlers397508044
pharmgkbrs397508044
gwascentralrs397508044
openSNPrs397508044
23andMers397508044
23andMe allrs397508044
SNP Nexus

SNPshotrs397508044
SNPdbers397508044
MSV3drs397508044
GWAS Ctlgrs397508044
Max Magnitude0
ClinVar
Risk rs397508044(A;A)
Alt rs397508044(A;A)
Reference rs397508044(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.32968860T>A
CLNSRC ClinVar
CLNACC RCV000045781.2,