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rs397508054

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508054(-;-)
Make rs397508054(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394906
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508054
ebirs397508054
HLIrs397508054
Exacrs397508054
Varsomers397508054
Maprs397508054
PheGenIrs397508054
hapmaprs397508054
1000 genomesrs397508054
hgdprs397508054
ensemblrs397508054
gopubmedrs397508054
geneviewrs397508054
scholarrs397508054
googlers397508054
pharmgkbrs397508054
gwascentralrs397508054
openSNPrs397508054
23andMers397508054
23andMe allrs397508054
SNP Nexus

SNPshotrs397508054
SNPdbers397508054
MSV3drs397508054
GWAS Ctlgrs397508054
Max Magnitude0
ClinVar
Risk rs397508054(;)
Alt rs397508054(;)
Reference rs397508054(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.32969043delA
CLNSRC ClinVar
CLNACC RCV000045830.2,