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rs793888534

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs793888534(A;A)
Make rs793888534(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114973
GenePURA
is asnp
is mentioned by
dbSNPrs793888534
ebirs793888534
HLIrs793888534
Exacrs793888534
Varsomers793888534
Maprs793888534
PheGenIrs793888534
hapmaprs793888534
1000 genomesrs793888534
hgdprs793888534
ensemblrs793888534
gopubmedrs793888534
geneviewrs793888534
scholarrs793888534
googlers793888534
pharmgkbrs793888534
gwascentralrs793888534
openSNPrs793888534
23andMers793888534
23andMe allrs793888534
SNP Nexus

SNPshotrs793888534
SNPdbers793888534
MSV3drs793888534
GWAS Ctlgrs793888534
Max Magnitude0
ClinVar
Risk rs793888534(A;A)
Alt rs793888534(A;A)
Reference rs793888534(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494558G>A
CLNSRC
CLNACC RCV000172936.1,