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rs72558444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558444(A;G)
Make rs72558444(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408948
GeneOTC
is asnp
is mentioned by
dbSNPrs72558444
ebirs72558444
HLIrs72558444
Exacrs72558444
Varsomers72558444
Maprs72558444
PheGenIrs72558444
hapmaprs72558444
1000 genomesrs72558444
hgdprs72558444
ensemblrs72558444
gopubmedrs72558444
geneviewrs72558444
scholarrs72558444
googlers72558444
pharmgkbrs72558444
gwascentralrs72558444
openSNPrs72558444
23andMers72558444
23andMe allrs72558444
SNP Nexus

SNPshotrs72558444
SNPdbers72558444
MSV3drs72558444
GWAS Ctlgrs72558444
Max Magnitude0
ClinVar
Risk rs72558444(G;G)
Alt rs72558444(G;G)
Reference rs72558444(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268201A>G
CLNSRC ClinVar
CLNACC RCV000083573.1,