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rs397508953

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508953(-;-)
Make rs397508953(-;C)
Make rs397508953(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093289
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508953
ebirs397508953
HLIrs397508953
Exacrs397508953
Varsomers397508953
Maprs397508953
PheGenIrs397508953
hapmaprs397508953
1000 genomesrs397508953
hgdprs397508953
ensemblrs397508953
gopubmedrs397508953
geneviewrs397508953
scholarrs397508953
googlers397508953
pharmgkbrs397508953
gwascentralrs397508953
openSNPrs397508953
23andMers397508953
23andMe allrs397508953
SNP Nexus

SNPshotrs397508953
SNPdbers397508953
MSV3drs397508953
GWAS Ctlgrs397508953
Max Magnitude0
ClinVar
Risk rs397508953(C;C)
Alt rs397508953(C;C)
Reference rs397508953(;)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245307dupG
CLNSRC ClinVar
CLNACC RCV000047771.2, RCV000077096.2,