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

rs397509340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509340(-;-)
Make rs397509340(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094570
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509340
ebirs397509340
HLIrs397509340
Exacrs397509340
Varsomers397509340
Maprs397509340
PheGenIrs397509340
hapmaprs397509340
1000 genomesrs397509340
hgdprs397509340
ensemblrs397509340
gopubmedrs397509340
geneviewrs397509340
scholarrs397509340
googlers397509340
pharmgkbrs397509340
gwascentralrs397509340
openSNPrs397509340
23andMers397509340
23andMe allrs397509340
SNP Nexus

SNPshotrs397509340
SNPdbers397509340
MSV3drs397509340
GWAS Ctlgrs397509340
Max Magnitude0
ClinVar
Risk rs397509340(;)
Alt rs397509340(;)
Reference rs397509340(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246587delA
CLNSRC ClinVar
CLNACC RCV000049203.2,