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

rs72554329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554329(G;T)
Make rs72554329(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369810
GeneOTC
is asnp
is mentioned by
dbSNPrs72554329
ebirs72554329
HLIrs72554329
Exacrs72554329
Varsomers72554329
Maprs72554329
PheGenIrs72554329
hapmaprs72554329
1000 genomesrs72554329
hgdprs72554329
ensemblrs72554329
gopubmedrs72554329
geneviewrs72554329
scholarrs72554329
googlers72554329
pharmgkbrs72554329
gwascentralrs72554329
openSNPrs72554329
23andMers72554329
23andMe allrs72554329
SNP Nexus

SNPshotrs72554329
SNPdbers72554329
MSV3drs72554329
GWAS Ctlgrs72554329
Max Magnitude0
ClinVar
Risk rs72554329(T;T)
Alt rs72554329(T;T)
Reference rs72554329(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229063G>T
CLNSRC ClinVar
CLNACC RCV000083367.1,