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rs72554319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554319(G;G)
Make rs72554319(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367376
GeneOTC
is asnp
is mentioned by
dbSNPrs72554319
ebirs72554319
HLIrs72554319
Exacrs72554319
Varsomers72554319
Maprs72554319
PheGenIrs72554319
hapmaprs72554319
1000 genomesrs72554319
hgdprs72554319
ensemblrs72554319
gopubmedrs72554319
geneviewrs72554319
scholarrs72554319
googlers72554319
pharmgkbrs72554319
gwascentralrs72554319
openSNPrs72554319
23andMers72554319
23andMe allrs72554319
SNP Nexus

SNPshotrs72554319
SNPdbers72554319
MSV3drs72554319
GWAS Ctlgrs72554319
Max Magnitude0
ClinVar
Risk rs72554319(G;G)
Alt rs72554319(G;G)
Reference rs72554319(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226629T>G
CLNSRC ClinVar
CLNACC RCV000083353.1,