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rs397508843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508843(-;-)
Make rs397508843(-;T)
Make rs397508843(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094371
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508843
ebirs397508843
HLIrs397508843
Exacrs397508843
Varsomers397508843
Maprs397508843
PheGenIrs397508843
hapmaprs397508843
1000 genomesrs397508843
hgdprs397508843
ensemblrs397508843
gopubmedrs397508843
geneviewrs397508843
scholarrs397508843
googlers397508843
pharmgkbrs397508843
gwascentralrs397508843
openSNPrs397508843
23andMers397508843
23andMe allrs397508843
SNP Nexus

SNPshotrs397508843
SNPdbers397508843
MSV3drs397508843
GWAS Ctlgrs397508843
Max Magnitude0
ClinVar
Risk rs397508843(T;T)
Alt rs397508843(T;T)
Reference rs397508843(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246389dupA
CLNSRC ClinVar
CLNACC RCV000047364.2,