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rs72556265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556265(G;G)
Make rs72556265(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401340
GeneOTC
is asnp
is mentioned by
dbSNPrs72556265
ebirs72556265
HLIrs72556265
Exacrs72556265
Varsomers72556265
Maprs72556265
PheGenIrs72556265
hapmaprs72556265
1000 genomesrs72556265
hgdprs72556265
ensemblrs72556265
gopubmedrs72556265
geneviewrs72556265
scholarrs72556265
googlers72556265
pharmgkbrs72556265
gwascentralrs72556265
openSNPrs72556265
23andMers72556265
23andMe allrs72556265
SNP Nexus

SNPshotrs72556265
SNPdbers72556265
MSV3drs72556265
GWAS Ctlgrs72556265
Max Magnitude0
ClinVar
Risk rs72556265(G;G)
Alt rs72556265(G;G)
Reference rs72556265(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260593T>G
CLNSRC ClinVar
CLNACC RCV000083444.1,