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

rs397509221

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509221(G;G)
Make rs397509221(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063959
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509221
ebirs397509221
HLIrs397509221
Exacrs397509221
Varsomers397509221
Maprs397509221
PheGenIrs397509221
hapmaprs397509221
1000 genomesrs397509221
hgdprs397509221
ensemblrs397509221
gopubmedrs397509221
geneviewrs397509221
scholarrs397509221
googlers397509221
pharmgkbrs397509221
gwascentralrs397509221
openSNPrs397509221
23andMers397509221
23andMe allrs397509221
SNP Nexus

SNPshotrs397509221
SNPdbers397509221
MSV3drs397509221
GWAS Ctlgrs397509221
Max Magnitude0
ClinVar
Risk rs397509221(G;G)
Alt rs397509221(G;G)
Reference rs397509221(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41215976A>C
CLNSRC ClinVar
CLNACC RCV000048775.2,