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rs397509065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509065(-;-)
Make rs397509065(-;T)
Make rs397509065(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092110
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509065
ebirs397509065
HLIrs397509065
Exacrs397509065
Varsomers397509065
Maprs397509065
PheGenIrs397509065
hapmaprs397509065
1000 genomesrs397509065
hgdprs397509065
ensemblrs397509065
gopubmedrs397509065
geneviewrs397509065
scholarrs397509065
googlers397509065
pharmgkbrs397509065
gwascentralrs397509065
openSNPrs397509065
23andMers397509065
23andMe allrs397509065
SNP Nexus

SNPshotrs397509065
SNPdbers397509065
MSV3drs397509065
GWAS Ctlgrs397509065
Max Magnitude0
ClinVar
Risk rs397509065(T;T)
Alt rs397509065(T;T)
Reference rs397509065(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244128dupA
CLNSRC ClinVar
CLNACC RCV000048189.2,