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rs793888536

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs793888536(C;C)
Make rs793888536(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114600
GenePURA
is asnp
is mentioned by
dbSNPrs793888536
ebirs793888536
HLIrs793888536
Exacrs793888536
Varsomers793888536
Maprs793888536
PheGenIrs793888536
hapmaprs793888536
1000 genomesrs793888536
hgdprs793888536
ensemblrs793888536
gopubmedrs793888536
geneviewrs793888536
scholarrs793888536
googlers793888536
pharmgkbrs793888536
gwascentralrs793888536
openSNPrs793888536
23andMers793888536
23andMe allrs793888536
SNP Nexus

SNPshotrs793888536
SNPdbers793888536
MSV3drs793888536
GWAS Ctlgrs793888536
Max Magnitude0
ClinVar
Risk rs793888536(C;C)
Alt rs793888536(C;C)
Reference rs793888536(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494185G>C
CLNSRC
CLNACC RCV000172938.2,