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rs397508874

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508874(-;-)
Make rs397508874(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094032
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508874
ebirs397508874
HLIrs397508874
Exacrs397508874
Varsomers397508874
Maprs397508874
PheGenIrs397508874
hapmaprs397508874
1000 genomesrs397508874
hgdprs397508874
ensemblrs397508874
gopubmedrs397508874
geneviewrs397508874
scholarrs397508874
googlers397508874
pharmgkbrs397508874
gwascentralrs397508874
openSNPrs397508874
23andMers397508874
23andMe allrs397508874
SNP Nexus

SNPshotrs397508874
SNPdbers397508874
MSV3drs397508874
GWAS Ctlgrs397508874
Max Magnitude0
ClinVar
Risk rs397508874(;)
Alt rs397508874(;)
Reference rs397508874(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.41246049delT
CLNSRC ClinVar
CLNACC RCV000047498.2,