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

rs397509174

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397509174(G;G)
Make rs397509174(G;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076555
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509174
ebirs397509174
HLIrs397509174
Exacrs397509174
Varsomers397509174
Maprs397509174
PheGenIrs397509174
hapmaprs397509174
1000 genomesrs397509174
hgdprs397509174
ensemblrs397509174
gopubmedrs397509174
geneviewrs397509174
scholarrs397509174
googlers397509174
pharmgkbrs397509174
gwascentralrs397509174
openSNPrs397509174
23andMers397509174
23andMe allrs397509174
SNP Nexus

SNPshotrs397509174
SNPdbers397509174
MSV3drs397509174
GWAS Ctlgrs397509174
Max Magnitude0
ClinVar
Risk rs397509174(G;G)
Alt rs397509174(G;G)
Reference rs397509174(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41228572_41228573delAAinsC
CLNSRC ClinVar
CLNACC RCV000048557.2,