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rs72554339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554339(A;T)
Make rs72554339(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369843
GeneOTC
is asnp
is mentioned by
dbSNPrs72554339
ebirs72554339
HLIrs72554339
Exacrs72554339
Varsomers72554339
Maprs72554339
PheGenIrs72554339
hapmaprs72554339
1000 genomesrs72554339
hgdprs72554339
ensemblrs72554339
gopubmedrs72554339
geneviewrs72554339
scholarrs72554339
googlers72554339
pharmgkbrs72554339
gwascentralrs72554339
openSNPrs72554339
23andMers72554339
23andMe allrs72554339
SNP Nexus

SNPshotrs72554339
SNPdbers72554339
MSV3drs72554339
GWAS Ctlgrs72554339
Max Magnitude0
ClinVar
Risk rs72554339(T;T)
Alt rs72554339(T;T)
Reference rs72554339(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229096A>T
CLNSRC ClinVar
CLNACC RCV000083377.1,