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rs72554305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554305(C;T)
Make rs72554305(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367319
GeneOTC
is asnp
is mentioned by
dbSNPrs72554305
ebirs72554305
HLIrs72554305
Exacrs72554305
Varsomers72554305
Maprs72554305
PheGenIrs72554305
hapmaprs72554305
1000 genomesrs72554305
hgdprs72554305
ensemblrs72554305
gopubmedrs72554305
geneviewrs72554305
scholarrs72554305
googlers72554305
pharmgkbrs72554305
gwascentralrs72554305
openSNPrs72554305
23andMers72554305
23andMe allrs72554305
SNP Nexus

SNPshotrs72554305
SNPdbers72554305
MSV3drs72554305
GWAS Ctlgrs72554305
Max Magnitude0
ClinVar
Risk rs72554305(G,T;G,T)
Alt rs72554305(G,T;G,T)
Reference rs72554305(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226572C>T
CLNSRC ClinVar
CLNACC RCV000083330.1,