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rs72558487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558487(C;C)
Make rs72558487(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421026
GeneOTC
is asnp
is mentioned by
dbSNPrs72558487
ebirs72558487
HLIrs72558487
Exacrs72558487
Varsomers72558487
Maprs72558487
PheGenIrs72558487
hapmaprs72558487
1000 genomesrs72558487
hgdprs72558487
ensemblrs72558487
gopubmedrs72558487
geneviewrs72558487
scholarrs72558487
googlers72558487
pharmgkbrs72558487
gwascentralrs72558487
openSNPrs72558487
23andMers72558487
23andMe allrs72558487
SNP Nexus

SNPshotrs72558487
SNPdbers72558487
MSV3drs72558487
GWAS Ctlgrs72558487
Max Magnitude0
ClinVar
Risk rs72558487(C;C)
Alt rs72558487(C;C)
Reference rs72558487(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280279G>C
CLNSRC ClinVar
CLNACC RCV000083319.1,