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rs72558488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558488(C;C)
Make rs72558488(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421032
GeneOTC
is asnp
is mentioned by
dbSNPrs72558488
ebirs72558488
HLIrs72558488
Exacrs72558488
Varsomers72558488
Maprs72558488
PheGenIrs72558488
hapmaprs72558488
1000 genomesrs72558488
hgdprs72558488
ensemblrs72558488
gopubmedrs72558488
geneviewrs72558488
scholarrs72558488
googlers72558488
pharmgkbrs72558488
gwascentralrs72558488
openSNPrs72558488
23andMers72558488
23andMe allrs72558488
SNP Nexus

SNPshotrs72558488
SNPdbers72558488
MSV3drs72558488
GWAS Ctlgrs72558488
Max Magnitude0
ClinVar
Risk rs72558488(C;C)
Alt rs72558488(C;C)
Reference rs72558488(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280285G>C
CLNSRC ClinVar
CLNACC RCV000083320.1,