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

rs397509334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509334(-;-)
Make rs397509334(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094622
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509334
ebirs397509334
HLIrs397509334
Exacrs397509334
Varsomers397509334
Maprs397509334
PheGenIrs397509334
hapmaprs397509334
1000 genomesrs397509334
hgdprs397509334
ensemblrs397509334
gopubmedrs397509334
geneviewrs397509334
scholarrs397509334
googlers397509334
pharmgkbrs397509334
gwascentralrs397509334
openSNPrs397509334
23andMers397509334
23andMe allrs397509334
SNP Nexus

SNPshotrs397509334
SNPdbers397509334
MSV3drs397509334
GWAS Ctlgrs397509334
Max Magnitude0
ClinVar
Risk rs397509334(;)
Alt rs397509334(;)
Reference rs397509334(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.41246639delT
CLNSRC ClinVar
CLNACC RCV000049185.2,