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

rs397508950

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397508950(-;-)
Make rs397508950(-;AG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093319
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508950
ebirs397508950
HLIrs397508950
Exacrs397508950
Varsomers397508950
Maprs397508950
PheGenIrs397508950
hapmaprs397508950
1000 genomesrs397508950
hgdprs397508950
ensemblrs397508950
gopubmedrs397508950
geneviewrs397508950
scholarrs397508950
googlers397508950
pharmgkbrs397508950
gwascentralrs397508950
openSNPrs397508950
23andMers397508950
23andMe allrs397508950
SNP Nexus

SNPshotrs397508950
SNPdbers397508950
MSV3drs397508950
GWAS Ctlgrs397508950
Max Magnitude0
ClinVar
Risk rs397508950(;)
Alt rs397508950(;)
Reference rs397508950(AG;AG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245336_41245337delCT
CLNSRC ClinVar
CLNACC RCV000047761.2,