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rs72556258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556258(A;A)
Make rs72556258(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401297
GeneOTC
is asnp
is mentioned by
dbSNPrs72556258
ebirs72556258
HLIrs72556258
Exacrs72556258
Varsomers72556258
Maprs72556258
PheGenIrs72556258
hapmaprs72556258
1000 genomesrs72556258
hgdprs72556258
ensemblrs72556258
gopubmedrs72556258
geneviewrs72556258
scholarrs72556258
googlers72556258
pharmgkbrs72556258
gwascentralrs72556258
openSNPrs72556258
23andMers72556258
23andMe allrs72556258
SNP Nexus

SNPshotrs72556258
SNPdbers72556258
MSV3drs72556258
GWAS Ctlgrs72556258
Max Magnitude0
ClinVar
Risk rs72556258(A;A)
Alt rs72556258(A;A)
Reference rs72556258(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260550G>A
CLNSRC ClinVar
CLNACC RCV000083428.1,