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rs793888539

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs793888539(-;-)
Make rs793888539(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114926
GenePURA
is asnp
is mentioned by
dbSNPrs793888539
ebirs793888539
HLIrs793888539
Exacrs793888539
Varsomers793888539
Maprs793888539
PheGenIrs793888539
hapmaprs793888539
1000 genomesrs793888539
hgdprs793888539
ensemblrs793888539
gopubmedrs793888539
geneviewrs793888539
scholarrs793888539
googlers793888539
pharmgkbrs793888539
gwascentralrs793888539
openSNPrs793888539
23andMers793888539
23andMe allrs793888539
SNP Nexus

SNPshotrs793888539
SNPdbers793888539
MSV3drs793888539
GWAS Ctlgrs793888539
Max Magnitude0
ClinVar
Risk rs793888539(;)
Alt rs793888539(;)
Reference rs793888539(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494511delG
CLNSRC
CLNACC RCV000172942.1,