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rs72554330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554330(C;T)
Make rs72554330(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369811
GeneOTC
is asnp
is mentioned by
dbSNPrs72554330
ebirs72554330
HLIrs72554330
Exacrs72554330
Varsomers72554330
Maprs72554330
PheGenIrs72554330
hapmaprs72554330
1000 genomesrs72554330
hgdprs72554330
ensemblrs72554330
gopubmedrs72554330
geneviewrs72554330
scholarrs72554330
googlers72554330
pharmgkbrs72554330
gwascentralrs72554330
openSNPrs72554330
23andMers72554330
23andMe allrs72554330
SNP Nexus

SNPshotrs72554330
SNPdbers72554330
MSV3drs72554330
GWAS Ctlgrs72554330
Max Magnitude0
ClinVar
Risk rs72554330(T;T)
Alt rs72554330(T;T)
Reference rs72554330(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229064C>T
CLNSRC ClinVar
CLNACC RCV000083368.1,