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rs397509155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509155(-;-)
Make rs397509155(-;T)
Make rs397509155(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082518
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509155
ebirs397509155
HLIrs397509155
Exacrs397509155
Varsomers397509155
Maprs397509155
PheGenIrs397509155
hapmaprs397509155
1000 genomesrs397509155
hgdprs397509155
ensemblrs397509155
gopubmedrs397509155
geneviewrs397509155
scholarrs397509155
googlers397509155
pharmgkbrs397509155
gwascentralrs397509155
openSNPrs397509155
23andMers397509155
23andMe allrs397509155
SNP Nexus

SNPshotrs397509155
SNPdbers397509155
MSV3drs397509155
GWAS Ctlgrs397509155
Max Magnitude0
ClinVar
Risk rs397509155(T;T)
Alt rs397509155(T;T)
Reference rs397509155(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41234535_41234536insA
CLNSRC ClinVar
CLNACC RCV000048497.2,