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

rs397509279

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509279(A;G)
Make rs397509279(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049117
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509279
ebirs397509279
HLIrs397509279
Exacrs397509279
Varsomers397509279
Maprs397509279
PheGenIrs397509279
hapmaprs397509279
1000 genomesrs397509279
hgdprs397509279
ensemblrs397509279
gopubmedrs397509279
geneviewrs397509279
scholarrs397509279
googlers397509279
pharmgkbrs397509279
gwascentralrs397509279
openSNPrs397509279
23andMers397509279
23andMe allrs397509279
SNP Nexus

SNPshotrs397509279
SNPdbers397509279
MSV3drs397509279
GWAS Ctlgrs397509279
Max Magnitude0
ClinVar
Risk rs397509279(G;G)
Alt rs397509279(G;G)
Reference rs397509279(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.41201134T>C
CLNSRC ClinVar
CLNACC RCV000048976.2,