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rs72554352

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554352(A;A)
Make rs72554352(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381359
GeneOTC
is asnp
is mentioned by
dbSNPrs72554352
ebirs72554352
HLIrs72554352
Exacrs72554352
Varsomers72554352
Maprs72554352
PheGenIrs72554352
hapmaprs72554352
1000 genomesrs72554352
hgdprs72554352
ensemblrs72554352
gopubmedrs72554352
geneviewrs72554352
scholarrs72554352
googlers72554352
pharmgkbrs72554352
gwascentralrs72554352
openSNPrs72554352
23andMers72554352
23andMe allrs72554352
SNP Nexus

SNPshotrs72554352
SNPdbers72554352
MSV3drs72554352
GWAS Ctlgrs72554352
Max Magnitude0
ClinVar
Risk rs72554352(A;A)
Alt rs72554352(A;A)
Reference rs72554352(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240612G>A
CLNSRC ClinVar
CLNACC RCV000083400.1,