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

rs397509209

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGGCCTGACCCCAGA;CTGGCCTGACCCCAGA) 0 common in clinvar
Make rs397509209(-;-)
Make rs397509209(-;CTGGCCTGACCCCAGA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070935
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509209
ebirs397509209
HLIrs397509209
Exacrs397509209
Varsomers397509209
Maprs397509209
PheGenIrs397509209
hapmaprs397509209
1000 genomesrs397509209
hgdprs397509209
ensemblrs397509209
gopubmedrs397509209
geneviewrs397509209
scholarrs397509209
googlers397509209
pharmgkbrs397509209
gwascentralrs397509209
openSNPrs397509209
23andMers397509209
23andMe allrs397509209
SNP Nexus

SNPshotrs397509209
SNPdbers397509209
MSV3drs397509209
GWAS Ctlgrs397509209
Max Magnitude0
ClinVar
Risk rs397509209(;)
Alt rs397509209(;)
Reference rs397509209(CTGGCCTGACCCCAGA;CTGGCCTGACCCCAGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41222952_41222967del16
CLNSRC ClinVar
CLNACC RCV000048713.2,