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rs72554325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554325(G;G)
Make rs72554325(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367413
GeneOTC
is asnp
is mentioned by
dbSNPrs72554325
ebirs72554325
HLIrs72554325
Exacrs72554325
Varsomers72554325
Maprs72554325
PheGenIrs72554325
hapmaprs72554325
1000 genomesrs72554325
hgdprs72554325
ensemblrs72554325
gopubmedrs72554325
geneviewrs72554325
scholarrs72554325
googlers72554325
pharmgkbrs72554325
gwascentralrs72554325
openSNPrs72554325
23andMers72554325
23andMe allrs72554325
SNP Nexus

SNPshotrs72554325
SNPdbers72554325
MSV3drs72554325
GWAS Ctlgrs72554325
Max Magnitude0
ClinVar
Risk rs72554325(G;G)
Alt rs72554325(G;G)
Reference rs72554325(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226666T>G
CLNSRC ClinVar
CLNACC RCV000083361.1,