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rs397509150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509150(A;A)
Make rs397509150(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082576
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509150
ebirs397509150
HLIrs397509150
Exacrs397509150
Varsomers397509150
Maprs397509150
PheGenIrs397509150
hapmaprs397509150
1000 genomesrs397509150
hgdprs397509150
ensemblrs397509150
gopubmedrs397509150
geneviewrs397509150
scholarrs397509150
googlers397509150
pharmgkbrs397509150
gwascentralrs397509150
openSNPrs397509150
23andMers397509150
23andMe allrs397509150
SNP Nexus

SNPshotrs397509150
SNPdbers397509150
MSV3drs397509150
GWAS Ctlgrs397509150
Max Magnitude0
ClinVar
Risk rs397509150(A;A)
Alt rs397509150(A;A)
Reference rs397509150(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.41234593C>T
CLNSRC ClinVar
CLNACC RCV000048480.2,