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rs72556290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556290(A;G)
Make rs72556290(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403619
GeneOTC
is asnp
is mentioned by
dbSNPrs72556290
ebirs72556290
HLIrs72556290
Exacrs72556290
Varsomers72556290
Maprs72556290
PheGenIrs72556290
hapmaprs72556290
1000 genomesrs72556290
hgdprs72556290
ensemblrs72556290
gopubmedrs72556290
geneviewrs72556290
scholarrs72556290
googlers72556290
pharmgkbrs72556290
gwascentralrs72556290
openSNPrs72556290
23andMers72556290
23andMe allrs72556290
SNP Nexus

SNPshotrs72556290
SNPdbers72556290
MSV3drs72556290
GWAS Ctlgrs72556290
Max Magnitude0
ClinVar
Risk rs72556290(G;G)
Alt rs72556290(G;G)
Reference rs72556290(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262872A>G
CLNSRC ClinVar
CLNACC RCV000083485.1,