Have questions? Visit https://www.reddit.com/r/SNPedia

rs793888537

From SNPedia

Orientationplus
Geno Mag Summary
(GCGGA;GCGGA) 0 common in clinvar
Make rs793888537(-;-)
Make rs793888537(-;GCGGA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114185
GenePURA
is asnp
is mentioned by
dbSNPrs793888537
ebirs793888537
HLIrs793888537
Exacrs793888537
Varsomers793888537
Maprs793888537
PheGenIrs793888537
hapmaprs793888537
1000 genomesrs793888537
hgdprs793888537
ensemblrs793888537
gopubmedrs793888537
geneviewrs793888537
scholarrs793888537
googlers793888537
pharmgkbrs793888537
gwascentralrs793888537
openSNPrs793888537
23andMers793888537
23andMe allrs793888537
SNP Nexus

SNPshotrs793888537
SNPdbers793888537
MSV3drs793888537
GWAS Ctlgrs793888537
Max Magnitude0
ClinVar
Risk rs793888537(;)
Alt rs793888537(;)
Reference rs793888537(GCGGA;GCGGA)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139493770_139493774delGCGGA
CLNSRC
CLNACC RCV000172940.1,