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rs72554335

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554335(G;G)
Make rs72554335(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369824
GeneOTC
is asnp
is mentioned by
dbSNPrs72554335
ebirs72554335
HLIrs72554335
Exacrs72554335
Varsomers72554335
Maprs72554335
PheGenIrs72554335
hapmaprs72554335
1000 genomesrs72554335
hgdprs72554335
ensemblrs72554335
gopubmedrs72554335
geneviewrs72554335
scholarrs72554335
googlers72554335
pharmgkbrs72554335
gwascentralrs72554335
openSNPrs72554335
23andMers72554335
23andMe allrs72554335
SNP Nexus

SNPshotrs72554335
SNPdbers72554335
MSV3drs72554335
GWAS Ctlgrs72554335
Max Magnitude0
ClinVar
Risk rs72554335(G;G)
Alt rs72554335(G;G)
Reference rs72554335(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229077T>G
CLNSRC ClinVar
CLNACC RCV000083373.1,