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rs793888528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs793888528(A;G)
Make rs793888528(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114864
GenePURA
is asnp
is mentioned by
dbSNPrs793888528
dbSNP (old)rs793888528
ClinGenrs793888528
ebirs793888528
HLIrs793888528
Exacrs793888528
Gnomadrs793888528
Varsomers793888528
Maprs793888528
PheGenIrs793888528
Biobankrs793888528
1000 genomesrs793888528
hgdprs793888528
ensemblrs793888528
gopubmedrs793888528
geneviewrs793888528
scholarrs793888528
googlers793888528
pharmgkbrs793888528
gwascentralrs793888528
openSNPrs793888528
23andMers793888528
23andMe allrs793888528
SNP Nexus

SNPshotrs793888528
SNPdbers793888528
MSV3drs793888528
GWAS Ctlgrs793888528
Max Magnitude0
ClinVar
Risk rs793888528(G;G)
Alt rs793888528(G;G)
Reference Rs793888528(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494449A>G
CLNSRC
CLNACC RCV000172930.2,