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rs72554311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554311(C;G)
Make rs72554311(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367346
GeneOTC
is asnp
is mentioned by
dbSNPrs72554311
ebirs72554311
HLIrs72554311
Exacrs72554311
Varsomers72554311
Maprs72554311
PheGenIrs72554311
hapmaprs72554311
1000 genomesrs72554311
hgdprs72554311
ensemblrs72554311
gopubmedrs72554311
geneviewrs72554311
scholarrs72554311
googlers72554311
pharmgkbrs72554311
gwascentralrs72554311
openSNPrs72554311
23andMers72554311
23andMe allrs72554311
SNP Nexus

SNPshotrs72554311
SNPdbers72554311
MSV3drs72554311
GWAS Ctlgrs72554311
Max Magnitude0
ClinVar
Risk rs72554311(G;G)
Alt rs72554311(G;G)
Reference rs72554311(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226599C>G
CLNSRC ClinVar
CLNACC RCV000083337.1,