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rs72558477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558477(G;T)
Make rs72558477(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411976
GeneOTC
is asnp
is mentioned by
dbSNPrs72558477
ebirs72558477
HLIrs72558477
Exacrs72558477
Varsomers72558477
Maprs72558477
PheGenIrs72558477
hapmaprs72558477
1000 genomesrs72558477
hgdprs72558477
ensemblrs72558477
gopubmedrs72558477
geneviewrs72558477
scholarrs72558477
googlers72558477
pharmgkbrs72558477
gwascentralrs72558477
openSNPrs72558477
23andMers72558477
23andMe allrs72558477
SNP Nexus

SNPshotrs72558477
SNPdbers72558477
MSV3drs72558477
GWAS Ctlgrs72558477
Max Magnitude0
ClinVar
Risk rs72558477(T;T)
Alt rs72558477(T;T)
Reference rs72558477(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271229G>T
CLNSRC ClinVar
CLNACC RCV000083624.1,