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rs72554334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
(D;D) 0
Make rs72554334(-;-)
Make rs72554334(-;CTT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369822
GeneOTC
is asnp
is mentioned by
dbSNPrs72554334
ebirs72554334
HLIrs72554334
Exacrs72554334
Varsomers72554334
Maprs72554334
PheGenIrs72554334
hapmaprs72554334
1000 genomesrs72554334
hgdprs72554334
ensemblrs72554334
gopubmedrs72554334
geneviewrs72554334
scholarrs72554334
googlers72554334
pharmgkbrs72554334
gwascentralrs72554334
openSNPrs72554334
23andMers72554334
23andMe allrs72554334
SNP Nexus

SNPshotrs72554334
SNPdbers72554334
MSV3drs72554334
GWAS Ctlgrs72554334
Max Magnitude0
ClinVar
Risk rs72554334(;)
Alt rs72554334(;)
Reference rs72554334(CTT;CTT)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229075_38229077delCTT
CLNSRC ClinVar
CLNACC RCV000083372.1,