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rs397508837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508837(-;-)
Make rs397508837(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094419
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508837
ebirs397508837
HLIrs397508837
Exacrs397508837
Varsomers397508837
Maprs397508837
PheGenIrs397508837
hapmaprs397508837
1000 genomesrs397508837
hgdprs397508837
ensemblrs397508837
gopubmedrs397508837
geneviewrs397508837
scholarrs397508837
googlers397508837
pharmgkbrs397508837
gwascentralrs397508837
openSNPrs397508837
23andMers397508837
23andMe allrs397508837
SNP Nexus

SNPshotrs397508837
SNPdbers397508837
MSV3drs397508837
GWAS Ctlgrs397508837
Max Magnitude0
ClinVar
Risk rs397508837(;)
Alt rs397508837(;)
Reference rs397508837(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246436delG
CLNSRC ClinVar
CLNACC RCV000047346.2,