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rs793888531

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs793888531(G;G)
Make rs793888531(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114486
GenePURA
is asnp
is mentioned by
dbSNPrs793888531
ebirs793888531
HLIrs793888531
Exacrs793888531
Varsomers793888531
Maprs793888531
PheGenIrs793888531
hapmaprs793888531
1000 genomesrs793888531
hgdprs793888531
ensemblrs793888531
gopubmedrs793888531
geneviewrs793888531
scholarrs793888531
googlers793888531
pharmgkbrs793888531
gwascentralrs793888531
openSNPrs793888531
23andMers793888531
23andMe allrs793888531
SNP Nexus

SNPshotrs793888531
SNPdbers793888531
MSV3drs793888531
GWAS Ctlgrs793888531
Max Magnitude0
ClinVar
Risk rs793888531(G;G)
Alt rs793888531(G;G)
Reference rs793888531(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494071T>G
CLNSRC
CLNACC RCV000172933.2,