Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509023

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509023(G;T)
Make rs397509023(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092617
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509023
ebirs397509023
HLIrs397509023
Exacrs397509023
Varsomers397509023
Maprs397509023
PheGenIrs397509023
hapmaprs397509023
1000 genomesrs397509023
hgdprs397509023
ensemblrs397509023
gopubmedrs397509023
geneviewrs397509023
scholarrs397509023
googlers397509023
pharmgkbrs397509023
gwascentralrs397509023
openSNPrs397509023
23andMers397509023
23andMe allrs397509023
SNP Nexus

SNPshotrs397509023
SNPdbers397509023
MSV3drs397509023
GWAS Ctlgrs397509023
Max Magnitude0
ClinVar
Risk rs397509023(T;T)
Alt rs397509023(T;T)
Reference rs397509023(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.41244634C>A
CLNSRC ClinVar
CLNACC RCV000048006.2,