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rs397509138

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509138(-;-)
Make rs397509138(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091437
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509138
ebirs397509138
HLIrs397509138
Exacrs397509138
Varsomers397509138
Maprs397509138
PheGenIrs397509138
hapmaprs397509138
1000 genomesrs397509138
hgdprs397509138
ensemblrs397509138
gopubmedrs397509138
geneviewrs397509138
scholarrs397509138
googlers397509138
pharmgkbrs397509138
gwascentralrs397509138
openSNPrs397509138
23andMers397509138
23andMe allrs397509138
SNP Nexus

SNPshotrs397509138
SNPdbers397509138
MSV3drs397509138
GWAS Ctlgrs397509138
Max Magnitude0
ClinVar
Risk rs397509138(;)
Alt rs397509138(;)
Reference rs397509138(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.41243454delA
CLNSRC ClinVar
CLNACC RCV000048440.2,