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rs72558416

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558416(A;A)
Make rs72558416(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403699
GeneOTC
is asnp
is mentioned by
dbSNPrs72558416
ebirs72558416
HLIrs72558416
Exacrs72558416
Varsomers72558416
Maprs72558416
PheGenIrs72558416
hapmaprs72558416
1000 genomesrs72558416
hgdprs72558416
ensemblrs72558416
gopubmedrs72558416
geneviewrs72558416
scholarrs72558416
googlers72558416
pharmgkbrs72558416
gwascentralrs72558416
openSNPrs72558416
23andMers72558416
23andMe allrs72558416
SNP Nexus

SNPshotrs72558416
SNPdbers72558416
MSV3drs72558416
GWAS Ctlgrs72558416
Max Magnitude0
ClinVar
Risk rs72558416(A,T;A,T)
Alt rs72558416(A,T;A,T)
Reference rs72558416(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262952G>A
CLNSRC ClinVar
CLNACC RCV000083517.1,