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rs397508905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508905(A;T)
Make rs397508905(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093790
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508905
ebirs397508905
HLIrs397508905
Exacrs397508905
Varsomers397508905
Maprs397508905
PheGenIrs397508905
hapmaprs397508905
1000 genomesrs397508905
hgdprs397508905
ensemblrs397508905
gopubmedrs397508905
geneviewrs397508905
scholarrs397508905
googlers397508905
pharmgkbrs397508905
gwascentralrs397508905
openSNPrs397508905
23andMers397508905
23andMe allrs397508905
SNP Nexus

SNPshotrs397508905
SNPdbers397508905
MSV3drs397508905
GWAS Ctlgrs397508905
Max Magnitude0
ClinVar
Risk rs397508905(T;T)
Alt rs397508905(T;T)
Reference rs397508905(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245807T>A
CLNSRC ClinVar
CLNACC RCV000047574.2,