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rs397509158

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509158(-;-)
Make rs397509158(-;G)
Make rs397509158(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082494
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509158
ebirs397509158
HLIrs397509158
Exacrs397509158
Varsomers397509158
Maprs397509158
PheGenIrs397509158
hapmaprs397509158
1000 genomesrs397509158
hgdprs397509158
ensemblrs397509158
gopubmedrs397509158
geneviewrs397509158
scholarrs397509158
googlers397509158
pharmgkbrs397509158
gwascentralrs397509158
openSNPrs397509158
23andMers397509158
23andMe allrs397509158
SNP Nexus

SNPshotrs397509158
SNPdbers397509158
MSV3drs397509158
GWAS Ctlgrs397509158
Max Magnitude0
ClinVar
Risk rs397509158(G;G)
Alt rs397509158(G;G)
Reference rs397509158(;)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41234512dupC
CLNSRC ClinVar
CLNACC RCV000048509.2, RCV000225677.1,