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

rs397509066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509066(C;TA)
Make rs397509066(TA;TA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092103
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509066
ebirs397509066
HLIrs397509066
Exacrs397509066
Varsomers397509066
Maprs397509066
PheGenIrs397509066
hapmaprs397509066
1000 genomesrs397509066
hgdprs397509066
ensemblrs397509066
gopubmedrs397509066
geneviewrs397509066
scholarrs397509066
googlers397509066
pharmgkbrs397509066
gwascentralrs397509066
openSNPrs397509066
23andMers397509066
23andMe allrs397509066
SNP Nexus

SNPshotrs397509066
SNPdbers397509066
MSV3drs397509066
GWAS Ctlgrs397509066
Max Magnitude0
ClinVar
Risk rs397509066(TA;TA)
Alt rs397509066(TA;TA)
Reference rs397509066(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244120delGinsTA
CLNSRC ClinVar
CLNACC RCV000048193.2,