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rs72558468

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558468(A;A)
Make rs72558468(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411925
GeneOTC
is asnp
is mentioned by
dbSNPrs72558468
ebirs72558468
HLIrs72558468
Exacrs72558468
Varsomers72558468
Maprs72558468
PheGenIrs72558468
hapmaprs72558468
1000 genomesrs72558468
hgdprs72558468
ensemblrs72558468
gopubmedrs72558468
geneviewrs72558468
scholarrs72558468
googlers72558468
pharmgkbrs72558468
gwascentralrs72558468
openSNPrs72558468
23andMers72558468
23andMe allrs72558468
SNP Nexus

SNPshotrs72558468
SNPdbers72558468
MSV3drs72558468
GWAS Ctlgrs72558468
Max Magnitude0
ClinVar
Risk rs72558468(A;A)
Alt rs72558468(A;A)
Reference rs72558468(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271178G>A
CLNSRC ClinVar
CLNACC RCV000083612.1,