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rs72554333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554333(G;T)
Make rs72554333(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369819
GeneOTC
is asnp
is mentioned by
dbSNPrs72554333
ebirs72554333
HLIrs72554333
Exacrs72554333
Varsomers72554333
Maprs72554333
PheGenIrs72554333
hapmaprs72554333
1000 genomesrs72554333
hgdprs72554333
ensemblrs72554333
gopubmedrs72554333
geneviewrs72554333
scholarrs72554333
googlers72554333
pharmgkbrs72554333
gwascentralrs72554333
openSNPrs72554333
23andMers72554333
23andMe allrs72554333
SNP Nexus

SNPshotrs72554333
SNPdbers72554333
MSV3drs72554333
GWAS Ctlgrs72554333
Max Magnitude0
ClinVar
Risk rs72554333(T;T)
Alt rs72554333(T;T)
Reference rs72554333(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229072G>T
CLNSRC ClinVar
CLNACC RCV000083371.1,