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rs72554321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554321(A;A)
Make rs72554321(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367383
GeneOTC
is asnp
is mentioned by
dbSNPrs72554321
ebirs72554321
HLIrs72554321
Exacrs72554321
Varsomers72554321
Maprs72554321
PheGenIrs72554321
hapmaprs72554321
1000 genomesrs72554321
hgdprs72554321
ensemblrs72554321
gopubmedrs72554321
geneviewrs72554321
scholarrs72554321
googlers72554321
pharmgkbrs72554321
gwascentralrs72554321
openSNPrs72554321
23andMers72554321
23andMe allrs72554321
SNP Nexus

SNPshotrs72554321
SNPdbers72554321
MSV3drs72554321
GWAS Ctlgrs72554321
Max Magnitude0
ClinVar
Risk rs72554321(A;A)
Alt rs72554321(A;A)
Reference rs72554321(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226636T>A
CLNSRC ClinVar
CLNACC RCV000083355.1,