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rs72556288

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556288(C;C)
Make rs72556288(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401429
GeneOTC
is asnp
is mentioned by
dbSNPrs72556288
ebirs72556288
HLIrs72556288
Exacrs72556288
Varsomers72556288
Maprs72556288
PheGenIrs72556288
hapmaprs72556288
1000 genomesrs72556288
hgdprs72556288
ensemblrs72556288
gopubmedrs72556288
geneviewrs72556288
scholarrs72556288
googlers72556288
pharmgkbrs72556288
gwascentralrs72556288
openSNPrs72556288
23andMers72556288
23andMe allrs72556288
SNP Nexus

SNPshotrs72556288
SNPdbers72556288
MSV3drs72556288
GWAS Ctlgrs72556288
Max Magnitude0
ClinVar
Risk rs72556288(C;C)
Alt rs72556288(C;C)
Reference rs72556288(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260682G>C
CLNSRC ClinVar
CLNACC RCV000083480.1,