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rs397509193

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509193(G;T)
Make rs397509193(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071173
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509193
ebirs397509193
HLIrs397509193
Exacrs397509193
Varsomers397509193
Maprs397509193
PheGenIrs397509193
hapmaprs397509193
1000 genomesrs397509193
hgdprs397509193
ensemblrs397509193
gopubmedrs397509193
geneviewrs397509193
scholarrs397509193
googlers397509193
pharmgkbrs397509193
gwascentralrs397509193
openSNPrs397509193
23andMers397509193
23andMe allrs397509193
SNP Nexus

SNPshotrs397509193
SNPdbers397509193
MSV3drs397509193
GWAS Ctlgrs397509193
Max Magnitude0
ClinVar
Risk rs397509193(T;T)
Alt rs397509193(T;T)
Reference rs397509193(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41223190C>A
CLNSRC ClinVar
CLNACC RCV000048647.2,