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rs72556292

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556292(G;G)
Make rs72556292(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403624
GeneOTC
is asnp
is mentioned by
dbSNPrs72556292
ebirs72556292
HLIrs72556292
Exacrs72556292
Varsomers72556292
Maprs72556292
PheGenIrs72556292
hapmaprs72556292
1000 genomesrs72556292
hgdprs72556292
ensemblrs72556292
gopubmedrs72556292
geneviewrs72556292
scholarrs72556292
googlers72556292
pharmgkbrs72556292
gwascentralrs72556292
openSNPrs72556292
23andMers72556292
23andMe allrs72556292
SNP Nexus

SNPshotrs72556292
SNPdbers72556292
MSV3drs72556292
GWAS Ctlgrs72556292
Max Magnitude0
ClinVar
Risk rs72556292(G;G)
Alt rs72556292(G;G)
Reference rs72556292(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262877T>G
CLNSRC ClinVar
CLNACC RCV000083487.1,