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rs793888535

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs793888535(C;C)
Make rs793888535(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114399
GenePURA
is asnp
is mentioned by
dbSNPrs793888535
ebirs793888535
HLIrs793888535
Exacrs793888535
Varsomers793888535
Maprs793888535
PheGenIrs793888535
hapmaprs793888535
1000 genomesrs793888535
hgdprs793888535
ensemblrs793888535
gopubmedrs793888535
geneviewrs793888535
scholarrs793888535
googlers793888535
pharmgkbrs793888535
gwascentralrs793888535
openSNPrs793888535
23andMers793888535
23andMe allrs793888535
SNP Nexus

SNPshotrs793888535
SNPdbers793888535
MSV3drs793888535
GWAS Ctlgrs793888535
Max Magnitude0
ClinVar
Risk rs793888535(C;C)
Alt rs793888535(C;C)
Reference rs793888535(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139493984T>C
CLNSRC
CLNACC RCV000172937.1,