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rs72554358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554358(A;G)
Make rs72554358(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381420
GeneOTC
is asnp
is mentioned by
dbSNPrs72554358
ebirs72554358
HLIrs72554358
Exacrs72554358
Varsomers72554358
Maprs72554358
PheGenIrs72554358
hapmaprs72554358
1000 genomesrs72554358
hgdprs72554358
ensemblrs72554358
gopubmedrs72554358
geneviewrs72554358
scholarrs72554358
googlers72554358
pharmgkbrs72554358
gwascentralrs72554358
openSNPrs72554358
23andMers72554358
23andMe allrs72554358
SNP Nexus

SNPshotrs72554358
SNPdbers72554358
MSV3drs72554358
GWAS Ctlgrs72554358
Max Magnitude0
ClinVar
Risk rs72554358(G;G)
Alt rs72554358(G;G)
Reference rs72554358(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240673A>G
CLNSRC ClinVar
CLNACC RCV000083410.1,