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rs72558469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
(I;I) 0
Make rs72558469(-;-)
Make rs72558469(-;GAA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411934
GeneOTC
is asnp
is mentioned by
dbSNPrs72558469
ebirs72558469
HLIrs72558469
Exacrs72558469
Varsomers72558469
Maprs72558469
PheGenIrs72558469
hapmaprs72558469
1000 genomesrs72558469
hgdprs72558469
ensemblrs72558469
gopubmedrs72558469
geneviewrs72558469
scholarrs72558469
googlers72558469
pharmgkbrs72558469
gwascentralrs72558469
openSNPrs72558469
23andMers72558469
23andMe allrs72558469
SNP Nexus

SNPshotrs72558469
SNPdbers72558469
MSV3drs72558469
GWAS Ctlgrs72558469
Max Magnitude0
ClinVar
Risk rs72558469(;)
Alt rs72558469(;)
Reference rs72558469(GAA;GAA)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271187_38271189delGAA
CLNSRC ClinVar
CLNACC RCV000083613.1,