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rs72554303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554303(C;G)
Make rs72554303(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367288
GeneOTC
is asnp
is mentioned by
dbSNPrs72554303
ebirs72554303
HLIrs72554303
Exacrs72554303
Varsomers72554303
Maprs72554303
PheGenIrs72554303
hapmaprs72554303
1000 genomesrs72554303
hgdprs72554303
ensemblrs72554303
gopubmedrs72554303
geneviewrs72554303
scholarrs72554303
googlers72554303
pharmgkbrs72554303
gwascentralrs72554303
openSNPrs72554303
23andMers72554303
23andMe allrs72554303
SNP Nexus

SNPshotrs72554303
SNPdbers72554303
MSV3drs72554303
GWAS Ctlgrs72554303
Max Magnitude0
ClinVar
Risk rs72554303(G;G)
Alt rs72554303(G;G)
Reference rs72554303(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226541C>G
CLNSRC ClinVar
CLNACC RCV000083568.1,