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rs72558442

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558442(A;A)
Make rs72558442(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408945
GeneOTC
is asnp
is mentioned by
dbSNPrs72558442
ebirs72558442
HLIrs72558442
Exacrs72558442
Varsomers72558442
Maprs72558442
PheGenIrs72558442
hapmaprs72558442
1000 genomesrs72558442
hgdprs72558442
ensemblrs72558442
gopubmedrs72558442
geneviewrs72558442
scholarrs72558442
googlers72558442
pharmgkbrs72558442
gwascentralrs72558442
openSNPrs72558442
23andMers72558442
23andMe allrs72558442
SNP Nexus

SNPshotrs72558442
SNPdbers72558442
MSV3drs72558442
GWAS Ctlgrs72558442
Max Magnitude0
ClinVar
Risk rs72558442(A;A)
Alt rs72558442(A;A)
Reference rs72558442(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268198G>A
CLNSRC ClinVar
CLNACC RCV000083571.1,