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rs72554344

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554344(A;G)
Make rs72554344(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369856
GeneOTC
is asnp
is mentioned by
dbSNPrs72554344
ebirs72554344
HLIrs72554344
Exacrs72554344
Varsomers72554344
Maprs72554344
PheGenIrs72554344
hapmaprs72554344
1000 genomesrs72554344
hgdprs72554344
ensemblrs72554344
gopubmedrs72554344
geneviewrs72554344
scholarrs72554344
googlers72554344
pharmgkbrs72554344
gwascentralrs72554344
openSNPrs72554344
23andMers72554344
23andMe allrs72554344
SNP Nexus

SNPshotrs72554344
SNPdbers72554344
MSV3drs72554344
GWAS Ctlgrs72554344
Max Magnitude0
ClinVar
Risk rs72554344(G;G)
Alt rs72554344(G;G)
Reference rs72554344(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229109A>G
CLNSRC ClinVar
CLNACC RCV000083387.1,