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rs72554324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554324(C;C)
Make rs72554324(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367401
GeneOTC
is asnp
is mentioned by
dbSNPrs72554324
ebirs72554324
HLIrs72554324
Exacrs72554324
Varsomers72554324
Maprs72554324
PheGenIrs72554324
hapmaprs72554324
1000 genomesrs72554324
hgdprs72554324
ensemblrs72554324
gopubmedrs72554324
geneviewrs72554324
scholarrs72554324
googlers72554324
pharmgkbrs72554324
gwascentralrs72554324
openSNPrs72554324
23andMers72554324
23andMe allrs72554324
SNP Nexus

SNPshotrs72554324
SNPdbers72554324
MSV3drs72554324
GWAS Ctlgrs72554324
Max Magnitude0
ClinVar
Risk rs72554324(C;C)
Alt rs72554324(C;C)
Reference rs72554324(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226654T>C
CLNSRC ClinVar
CLNACC RCV000083358.1,