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

rs793888529

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs793888529(A;T)
Make rs793888529(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114977
GenePURA
is asnp
is mentioned by
dbSNPrs793888529
ebirs793888529
HLIrs793888529
Exacrs793888529
Varsomers793888529
Maprs793888529
PheGenIrs793888529
hapmaprs793888529
1000 genomesrs793888529
hgdprs793888529
ensemblrs793888529
gopubmedrs793888529
geneviewrs793888529
scholarrs793888529
googlers793888529
pharmgkbrs793888529
gwascentralrs793888529
openSNPrs793888529
23andMers793888529
23andMe allrs793888529
SNP Nexus

SNPshotrs793888529
SNPdbers793888529
MSV3drs793888529
GWAS Ctlgrs793888529
Max Magnitude0
ClinVar
Risk rs793888529(T;T)
Alt rs793888529(T;T)
Reference rs793888529(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PURA
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.139494562A>T
CLNSRC
CLNACC RCV000172931.2,