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rs397508842

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397508842(-;-)
Make rs397508842(-;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094372
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508842
ebirs397508842
HLIrs397508842
Exacrs397508842
Varsomers397508842
Maprs397508842
PheGenIrs397508842
hapmaprs397508842
1000 genomesrs397508842
hgdprs397508842
ensemblrs397508842
gopubmedrs397508842
geneviewrs397508842
scholarrs397508842
googlers397508842
pharmgkbrs397508842
gwascentralrs397508842
openSNPrs397508842
23andMers397508842
23andMe allrs397508842
SNP Nexus

SNPshotrs397508842
SNPdbers397508842
MSV3drs397508842
GWAS Ctlgrs397508842
Max Magnitude0
ClinVar
Risk rs397508842(;)
Alt rs397508842(;)
Reference rs397508842(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246389_41246390delAA
CLNSRC ClinVar
CLNACC RCV000047363.2,