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rs72554349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554349(A;A)
Make rs72554349(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381342
GeneOTC
is asnp
is mentioned by
dbSNPrs72554349
ebirs72554349
HLIrs72554349
Exacrs72554349
Varsomers72554349
Maprs72554349
PheGenIrs72554349
hapmaprs72554349
1000 genomesrs72554349
hgdprs72554349
ensemblrs72554349
gopubmedrs72554349
geneviewrs72554349
scholarrs72554349
googlers72554349
pharmgkbrs72554349
gwascentralrs72554349
openSNPrs72554349
23andMers72554349
23andMe allrs72554349
SNP Nexus

SNPshotrs72554349
SNPdbers72554349
MSV3drs72554349
GWAS Ctlgrs72554349
Max Magnitude0
ClinVar
Risk rs72554349(A;A)
Alt rs72554349(A;A)
Reference rs72554349(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240595G>A
CLNSRC ClinVar
CLNACC RCV000083396.2,