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

rs397509199

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509199(-;-)
Make rs397509199(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071077
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509199
ebirs397509199
HLIrs397509199
Exacrs397509199
Varsomers397509199
Maprs397509199
PheGenIrs397509199
hapmaprs397509199
1000 genomesrs397509199
hgdprs397509199
ensemblrs397509199
gopubmedrs397509199
geneviewrs397509199
scholarrs397509199
googlers397509199
pharmgkbrs397509199
gwascentralrs397509199
openSNPrs397509199
23andMers397509199
23andMe allrs397509199
SNP Nexus

SNPshotrs397509199
SNPdbers397509199
MSV3drs397509199
GWAS Ctlgrs397509199
Max Magnitude0
ClinVar
Risk rs397509199(;)
Alt rs397509199(;)
Reference rs397509199(A;A)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41223094delT
CLNSRC ClinVar
CLNACC RCV000048674.2, RCV000225385.1,