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rs397508878

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508878(-;-)
Make rs397508878(-;T)
Make rs397508878(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094017
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508878
ebirs397508878
HLIrs397508878
Exacrs397508878
Varsomers397508878
Maprs397508878
PheGenIrs397508878
hapmaprs397508878
1000 genomesrs397508878
hgdprs397508878
ensemblrs397508878
gopubmedrs397508878
geneviewrs397508878
scholarrs397508878
googlers397508878
pharmgkbrs397508878
gwascentralrs397508878
openSNPrs397508878
23andMers397508878
23andMe allrs397508878
SNP Nexus

SNPshotrs397508878
SNPdbers397508878
MSV3drs397508878
GWAS Ctlgrs397508878
Max Magnitude0
ClinVar
Risk rs397508878(T;T)
Alt rs397508878(T;T)
Reference rs397508878(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246034_41246035insA
CLNSRC ClinVar
CLNACC RCV000047510.2,