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rs72558486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558486(G;T)
Make rs72558486(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421023
GeneOTC
is asnp
is mentioned by
dbSNPrs72558486
ebirs72558486
HLIrs72558486
Exacrs72558486
Varsomers72558486
Maprs72558486
PheGenIrs72558486
hapmaprs72558486
1000 genomesrs72558486
hgdprs72558486
ensemblrs72558486
gopubmedrs72558486
geneviewrs72558486
scholarrs72558486
googlers72558486
pharmgkbrs72558486
gwascentralrs72558486
openSNPrs72558486
23andMers72558486
23andMe allrs72558486
SNP Nexus

SNPshotrs72558486
SNPdbers72558486
MSV3drs72558486
GWAS Ctlgrs72558486
Max Magnitude0
ClinVar
Risk rs72558486(T;T)
Alt rs72558486(T;T)
Reference rs72558486(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280276G>T
CLNSRC ClinVar
CLNACC RCV000083318.1,