Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509068(-;-)
Make rs397509068(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092081
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509068
ebirs397509068
HLIrs397509068
Exacrs397509068
Varsomers397509068
Maprs397509068
PheGenIrs397509068
hapmaprs397509068
1000 genomesrs397509068
hgdprs397509068
ensemblrs397509068
gopubmedrs397509068
geneviewrs397509068
scholarrs397509068
googlers397509068
pharmgkbrs397509068
gwascentralrs397509068
openSNPrs397509068
23andMers397509068
23andMe allrs397509068
SNP Nexus

SNPshotrs397509068
SNPdbers397509068
MSV3drs397509068
GWAS Ctlgrs397509068
Max Magnitude0
ClinVar
Risk rs397509068(;)
Alt rs397509068(;)
Reference rs397509068(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244098delA
CLNSRC ClinVar
CLNACC RCV000048201.2,