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rs72558438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGTTGCTGA;TGTTGCTGA) 0 common in clinvar
Make rs72558438(-;-)
Make rs72558438(-;TGTTGCTGA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408889
GeneOTC
is asnp
is mentioned by
dbSNPrs72558438
ebirs72558438
HLIrs72558438
Exacrs72558438
Varsomers72558438
Maprs72558438
PheGenIrs72558438
hapmaprs72558438
1000 genomesrs72558438
hgdprs72558438
ensemblrs72558438
gopubmedrs72558438
geneviewrs72558438
scholarrs72558438
googlers72558438
pharmgkbrs72558438
gwascentralrs72558438
openSNPrs72558438
23andMers72558438
23andMe allrs72558438
SNP Nexus

SNPshotrs72558438
SNPdbers72558438
MSV3drs72558438
GWAS Ctlgrs72558438
Max Magnitude0
ClinVar
Risk rs72558438(;)
Alt rs72558438(;)
Reference rs72558438(TGTTGCTGA;TGTTGCTGA)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268142_38268150delTGTTGCTGA
CLNSRC ClinVar
CLNACC RCV000083553.1,