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rs397509026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509026(-;-)
Make rs397509026(-;T)
Make rs397509026(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092578
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509026
ebirs397509026
HLIrs397509026
Exacrs397509026
Varsomers397509026
Maprs397509026
PheGenIrs397509026
hapmaprs397509026
1000 genomesrs397509026
hgdprs397509026
ensemblrs397509026
gopubmedrs397509026
geneviewrs397509026
scholarrs397509026
googlers397509026
pharmgkbrs397509026
gwascentralrs397509026
openSNPrs397509026
23andMers397509026
23andMe allrs397509026
SNP Nexus

SNPshotrs397509026
SNPdbers397509026
MSV3drs397509026
GWAS Ctlgrs397509026
Max Magnitude0
ClinVar
Risk rs397509026(T;T)
Alt rs397509026(T;T)
Reference rs397509026(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244596dupA
CLNSRC ClinVar
CLNACC RCV000048022.2,