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rs397509154

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509154(-;-)
Make rs397509154(-;C)
Make rs397509154(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082520
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509154
ebirs397509154
HLIrs397509154
Exacrs397509154
Varsomers397509154
Maprs397509154
PheGenIrs397509154
hapmaprs397509154
1000 genomesrs397509154
hgdprs397509154
ensemblrs397509154
gopubmedrs397509154
geneviewrs397509154
scholarrs397509154
googlers397509154
pharmgkbrs397509154
gwascentralrs397509154
openSNPrs397509154
23andMers397509154
23andMe allrs397509154
SNP Nexus

SNPshotrs397509154
SNPdbers397509154
MSV3drs397509154
GWAS Ctlgrs397509154
Max Magnitude0
ClinVar
Risk rs397509154(C;C)
Alt rs397509154(C;C)
Reference rs397509154(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41234538dupG
CLNSRC ClinVar
CLNACC RCV000048496.2,