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rs797044866

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044866(G;T)
Make rs797044866(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140114653
GenePURA
is asnp
is mentioned by
dbSNPrs797044866
ebirs797044866
HLIrs797044866
Exacrs797044866
Varsomers797044866
Maprs797044866
PheGenIrs797044866
hapmaprs797044866
1000 genomesrs797044866
hgdprs797044866
ensemblrs797044866
gopubmedrs797044866
geneviewrs797044866
scholarrs797044866
googlers797044866
pharmgkbrs797044866
gwascentralrs797044866
openSNPrs797044866
23andMers797044866
23andMe allrs797044866
SNP Nexus

SNPshotrs797044866
SNPdbers797044866
MSV3drs797044866
GWAS Ctlgrs797044866
Max Magnitude0
ClinVar
Risk rs797044866(T;T)
Alt rs797044866(T;T)
Reference rs797044866(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PURA
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000005.9:g.139494238G>T
CLNSRC
CLNACC RCV000190672.1,