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rs72554336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554336(C;C)
Make rs72554336(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369826
GeneOTC
is asnp
is mentioned by
dbSNPrs72554336
ebirs72554336
HLIrs72554336
Exacrs72554336
Varsomers72554336
Maprs72554336
PheGenIrs72554336
hapmaprs72554336
1000 genomesrs72554336
hgdprs72554336
ensemblrs72554336
gopubmedrs72554336
geneviewrs72554336
scholarrs72554336
googlers72554336
pharmgkbrs72554336
gwascentralrs72554336
openSNPrs72554336
23andMers72554336
23andMe allrs72554336
SNP Nexus

SNPshotrs72554336
SNPdbers72554336
MSV3drs72554336
GWAS Ctlgrs72554336
Max Magnitude0
ClinVar
Risk rs72554336(C;C)
Alt rs72554336(C;C)
Reference rs72554336(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229079G>C
CLNSRC ClinVar
CLNACC RCV000083374.1,