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rs72554306

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554306(G;T)
Make rs72554306(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367328
GeneOTC
is asnp
is mentioned by
dbSNPrs72554306
ebirs72554306
HLIrs72554306
Exacrs72554306
Varsomers72554306
Maprs72554306
PheGenIrs72554306
hapmaprs72554306
1000 genomesrs72554306
hgdprs72554306
ensemblrs72554306
gopubmedrs72554306
geneviewrs72554306
scholarrs72554306
googlers72554306
pharmgkbrs72554306
gwascentralrs72554306
openSNPrs72554306
23andMers72554306
23andMe allrs72554306
SNP Nexus

SNPshotrs72554306
SNPdbers72554306
MSV3drs72554306
GWAS Ctlgrs72554306
Max Magnitude0
ClinVar
Risk rs72554306(T;T)
Alt rs72554306(T;T)
Reference rs72554306(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226581G>T
CLNSRC ClinVar
CLNACC RCV000083331.1,