Have questions? Visit https://www.reddit.com/r/SNPedia

rs72554320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554320(C;C)
Make rs72554320(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367380
GeneOTC
is asnp
is mentioned by
dbSNPrs72554320
ebirs72554320
HLIrs72554320
Exacrs72554320
Varsomers72554320
Maprs72554320
PheGenIrs72554320
hapmaprs72554320
1000 genomesrs72554320
hgdprs72554320
ensemblrs72554320
gopubmedrs72554320
geneviewrs72554320
scholarrs72554320
googlers72554320
pharmgkbrs72554320
gwascentralrs72554320
openSNPrs72554320
23andMers72554320
23andMe allrs72554320
SNP Nexus

SNPshotrs72554320
SNPdbers72554320
MSV3drs72554320
GWAS Ctlgrs72554320
Max Magnitude0
ClinVar
Risk rs72554320(C;C)
Alt rs72554320(C;C)
Reference rs72554320(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226633T>C
CLNSRC ClinVar
CLNACC RCV000083354.1,