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rs397509035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509035(C;G)
Make rs397509035(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092409
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509035
ebirs397509035
HLIrs397509035
Exacrs397509035
Varsomers397509035
Maprs397509035
PheGenIrs397509035
hapmaprs397509035
1000 genomesrs397509035
hgdprs397509035
ensemblrs397509035
gopubmedrs397509035
geneviewrs397509035
scholarrs397509035
googlers397509035
pharmgkbrs397509035
gwascentralrs397509035
openSNPrs397509035
23andMers397509035
23andMe allrs397509035
SNP Nexus

SNPshotrs397509035
SNPdbers397509035
MSV3drs397509035
GWAS Ctlgrs397509035
Max Magnitude0
ClinVar
Risk rs397509035(G;G)
Alt rs397509035(G;G)
Reference rs397509035(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.41244426G>C
CLNSRC ClinVar
CLNACC RCV000048075.2,