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

rs397509149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGTA;GGTA) 0 common in clinvar
Make rs397509149(-;-)
Make rs397509149(-;GGTA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43090941
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509149
ebirs397509149
HLIrs397509149
Exacrs397509149
Varsomers397509149
Maprs397509149
PheGenIrs397509149
hapmaprs397509149
1000 genomesrs397509149
hgdprs397509149
ensemblrs397509149
gopubmedrs397509149
geneviewrs397509149
scholarrs397509149
googlers397509149
pharmgkbrs397509149
gwascentralrs397509149
openSNPrs397509149
23andMers397509149
23andMe allrs397509149
SNP Nexus

SNPshotrs397509149
SNPdbers397509149
MSV3drs397509149
GWAS Ctlgrs397509149
Max Magnitude0
ClinVar
Risk rs397509149(;)
Alt rs397509149(;)
Reference rs397509149(GGTA;GGTA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41242958_41242961delTACC
CLNSRC ClinVar
CLNACC RCV000048478.2,