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rs793888532

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs793888532(-;-)
Make rs793888532(-;C)
Make rs793888532(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114949
GenePURA
is asnp
is mentioned by
dbSNPrs793888532
ebirs793888532
HLIrs793888532
Exacrs793888532
Varsomers793888532
Maprs793888532
PheGenIrs793888532
hapmaprs793888532
1000 genomesrs793888532
hgdprs793888532
ensemblrs793888532
gopubmedrs793888532
geneviewrs793888532
scholarrs793888532
googlers793888532
pharmgkbrs793888532
gwascentralrs793888532
openSNPrs793888532
23andMers793888532
23andMe allrs793888532
SNP Nexus

SNPshotrs793888532
SNPdbers793888532
MSV3drs793888532
GWAS Ctlgrs793888532
Max Magnitude0
ClinVar
Risk rs793888532(C;C)
Alt rs793888532(C;C)
Reference rs793888532(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494534dupC
CLNSRC
CLNACC RCV000172934.1,