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rs72554322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554322(A;A)
Make rs72554322(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367387
GeneOTC
is asnp
is mentioned by
dbSNPrs72554322
ebirs72554322
HLIrs72554322
Exacrs72554322
Varsomers72554322
Maprs72554322
PheGenIrs72554322
hapmaprs72554322
1000 genomesrs72554322
hgdprs72554322
ensemblrs72554322
gopubmedrs72554322
geneviewrs72554322
scholarrs72554322
googlers72554322
pharmgkbrs72554322
gwascentralrs72554322
openSNPrs72554322
23andMers72554322
23andMe allrs72554322
SNP Nexus

SNPshotrs72554322
SNPdbers72554322
MSV3drs72554322
GWAS Ctlgrs72554322
Max Magnitude0
ClinVar
Risk rs72554322(A;A)
Alt rs72554322(A;A)
Reference rs72554322(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226640G>A
CLNSRC ClinVar
CLNACC RCV000083356.1,