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rs397508829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508829(A;T)
Make rs397508829(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094468
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508829
ebirs397508829
HLIrs397508829
Exacrs397508829
Varsomers397508829
Maprs397508829
PheGenIrs397508829
hapmaprs397508829
1000 genomesrs397508829
hgdprs397508829
ensemblrs397508829
gopubmedrs397508829
geneviewrs397508829
scholarrs397508829
googlers397508829
pharmgkbrs397508829
gwascentralrs397508829
openSNPrs397508829
23andMers397508829
23andMe allrs397508829
SNP Nexus

SNPshotrs397508829
SNPdbers397508829
MSV3drs397508829
GWAS Ctlgrs397508829
Max Magnitude0
ClinVar
Risk rs397508829(C,T;C,T)
Alt rs397508829(C,T;C,T)
Reference rs397508829(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.41246485T>A
CLNSRC ClinVar
CLNACC RCV000047322.2,