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rs72554351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554351(G;T)
Make rs72554351(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381357
GeneOTC
is asnp
is mentioned by
dbSNPrs72554351
ebirs72554351
HLIrs72554351
Exacrs72554351
Varsomers72554351
Maprs72554351
PheGenIrs72554351
hapmaprs72554351
1000 genomesrs72554351
hgdprs72554351
ensemblrs72554351
gopubmedrs72554351
geneviewrs72554351
scholarrs72554351
googlers72554351
pharmgkbrs72554351
gwascentralrs72554351
openSNPrs72554351
23andMers72554351
23andMe allrs72554351
SNP Nexus

SNPshotrs72554351
SNPdbers72554351
MSV3drs72554351
GWAS Ctlgrs72554351
Max Magnitude0
ClinVar
Risk rs72554351(T;T)
Alt rs72554351(T;T)
Reference rs72554351(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240610G>T
CLNSRC ClinVar
CLNACC RCV000083399.1,