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rs397509153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509153(G;T)
Make rs397509153(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082524
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509153
ebirs397509153
HLIrs397509153
Exacrs397509153
Varsomers397509153
Maprs397509153
PheGenIrs397509153
hapmaprs397509153
1000 genomesrs397509153
hgdprs397509153
ensemblrs397509153
gopubmedrs397509153
geneviewrs397509153
scholarrs397509153
googlers397509153
pharmgkbrs397509153
gwascentralrs397509153
openSNPrs397509153
23andMers397509153
23andMe allrs397509153
SNP Nexus

SNPshotrs397509153
SNPdbers397509153
MSV3drs397509153
GWAS Ctlgrs397509153
Max Magnitude0
ClinVar
Risk rs397509153(T;T)
Alt rs397509153(T;T)
Reference rs397509153(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.41234541C>A
CLNSRC ClinVar
CLNACC RCV000048495.2,