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rs72558435

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558435(C;T)
Make rs72558435(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408883
GeneOTC
is asnp
is mentioned by
dbSNPrs72558435
ClinGenrs72558435
ebirs72558435
HLIrs72558435
Exacrs72558435
Varsomers72558435
Maprs72558435
PheGenIrs72558435
hapmaprs72558435
1000 genomesrs72558435
hgdprs72558435
ensemblrs72558435
gopubmedrs72558435
geneviewrs72558435
scholarrs72558435
googlers72558435
pharmgkbrs72558435
gwascentralrs72558435
openSNPrs72558435
23andMers72558435
23andMe allrs72558435
SNP Nexus

SNPshotrs72558435
SNPdbers72558435
MSV3drs72558435
GWAS Ctlgrs72558435
Max Magnitude0
ClinVar
Risk rs72558435(A;A) rs72558435(T;T)
Alt rs72558435(A;A) rs72558435(T;T)
Reference Rs72558435(C;C)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene OTC
CLNDBN not specified not provided
Reversed 0
HGVS NC_000023.10:g.38268136C>A; NC_000023.10:g.38268136C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000153627.3, RCV000083551.1,