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rs72556254

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556254(C;T)
Make rs72556254(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401283
GeneOTC
is asnp
is mentioned by
dbSNPrs72556254
ebirs72556254
HLIrs72556254
Exacrs72556254
Varsomers72556254
Maprs72556254
PheGenIrs72556254
hapmaprs72556254
1000 genomesrs72556254
hgdprs72556254
ensemblrs72556254
gopubmedrs72556254
geneviewrs72556254
scholarrs72556254
googlers72556254
pharmgkbrs72556254
gwascentralrs72556254
openSNPrs72556254
23andMers72556254
23andMe allrs72556254
SNP Nexus

SNPshotrs72556254
SNPdbers72556254
MSV3drs72556254
GWAS Ctlgrs72556254
Max Magnitude0
ClinVar
Risk rs72556254(T;T)
Alt rs72556254(T;T)
Reference rs72556254(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260536C>T
CLNSRC ClinVar
CLNACC RCV000083423.1,