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rs72554342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554342(G;G)
Make rs72554342(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369849
GeneOTC
is asnp
is mentioned by
dbSNPrs72554342
ebirs72554342
HLIrs72554342
Exacrs72554342
Varsomers72554342
Maprs72554342
PheGenIrs72554342
hapmaprs72554342
1000 genomesrs72554342
hgdprs72554342
ensemblrs72554342
gopubmedrs72554342
geneviewrs72554342
scholarrs72554342
googlers72554342
pharmgkbrs72554342
gwascentralrs72554342
openSNPrs72554342
23andMers72554342
23andMe allrs72554342
SNP Nexus

SNPshotrs72554342
SNPdbers72554342
MSV3drs72554342
GWAS Ctlgrs72554342
Max Magnitude0
ClinVar
Risk rs72554342(G;G)
Alt rs72554342(G;G)
Reference rs72554342(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229102T>G
CLNSRC ClinVar
CLNACC RCV000083380.1,