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rs72556294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556294(C;C)
Make rs72556294(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403639
GeneOTC
is asnp
is mentioned by
dbSNPrs72556294
ebirs72556294
HLIrs72556294
Exacrs72556294
Varsomers72556294
Maprs72556294
PheGenIrs72556294
hapmaprs72556294
1000 genomesrs72556294
hgdprs72556294
ensemblrs72556294
gopubmedrs72556294
geneviewrs72556294
scholarrs72556294
googlers72556294
pharmgkbrs72556294
gwascentralrs72556294
openSNPrs72556294
23andMers72556294
23andMe allrs72556294
SNP Nexus

SNPshotrs72556294
SNPdbers72556294
MSV3drs72556294
GWAS Ctlgrs72556294
Max Magnitude0
ClinVar
Risk rs72556294(C;C)
Alt rs72556294(C;C)
Reference rs72556294(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262892G>C
CLNSRC ClinVar
CLNACC RCV000083489.1,