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rs72558476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558476(A;A)
Make rs72558476(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411970
GeneOTC
is asnp
is mentioned by
dbSNPrs72558476
ebirs72558476
HLIrs72558476
Exacrs72558476
Varsomers72558476
Maprs72558476
PheGenIrs72558476
hapmaprs72558476
1000 genomesrs72558476
hgdprs72558476
ensemblrs72558476
gopubmedrs72558476
geneviewrs72558476
scholarrs72558476
googlers72558476
pharmgkbrs72558476
gwascentralrs72558476
openSNPrs72558476
23andMers72558476
23andMe allrs72558476
SNP Nexus

SNPshotrs72558476
SNPdbers72558476
MSV3drs72558476
GWAS Ctlgrs72558476
Max Magnitude0
ClinVar
Risk rs72558476(A;A)
Alt rs72558476(A;A)
Reference rs72558476(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271223G>A
CLNSRC ClinVar
CLNACC RCV000083623.1,