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

rs397509098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509098(A;A)
Make rs397509098(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091778
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509098
ebirs397509098
HLIrs397509098
Exacrs397509098
Varsomers397509098
Maprs397509098
PheGenIrs397509098
hapmaprs397509098
1000 genomesrs397509098
hgdprs397509098
ensemblrs397509098
gopubmedrs397509098
geneviewrs397509098
scholarrs397509098
googlers397509098
pharmgkbrs397509098
gwascentralrs397509098
openSNPrs397509098
23andMers397509098
23andMe allrs397509098
SNP Nexus

SNPshotrs397509098
SNPdbers397509098
MSV3drs397509098
GWAS Ctlgrs397509098
Max Magnitude0
ClinVar
Risk rs397509098(A;A)
Alt rs397509098(A;A)
Reference rs397509098(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.41243795A>T
CLNSRC ClinVar
CLNACC RCV000048312.2,