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rs397509171

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509171(C;T)
Make rs397509171(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076573
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509171
ebirs397509171
HLIrs397509171
Exacrs397509171
Varsomers397509171
Maprs397509171
PheGenIrs397509171
hapmaprs397509171
1000 genomesrs397509171
hgdprs397509171
ensemblrs397509171
gopubmedrs397509171
geneviewrs397509171
scholarrs397509171
googlers397509171
pharmgkbrs397509171
gwascentralrs397509171
openSNPrs397509171
23andMers397509171
23andMe allrs397509171
SNP Nexus

SNPshotrs397509171
SNPdbers397509171
MSV3drs397509171
GWAS Ctlgrs397509171
Max Magnitude0
ClinVar
Risk rs397509171(T;T)
Alt rs397509171(T;T)
Reference rs397509171(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41228590G>A
CLNSRC ClinVar
CLNACC RCV000048551.2,