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rs72554304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554304(C;T)
Make rs72554304(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367307
GeneOTC
is asnp
is mentioned by
dbSNPrs72554304
ebirs72554304
HLIrs72554304
Exacrs72554304
Varsomers72554304
Maprs72554304
PheGenIrs72554304
hapmaprs72554304
1000 genomesrs72554304
hgdprs72554304
ensemblrs72554304
gopubmedrs72554304
geneviewrs72554304
scholarrs72554304
googlers72554304
pharmgkbrs72554304
gwascentralrs72554304
openSNPrs72554304
23andMers72554304
23andMe allrs72554304
SNP Nexus

SNPshotrs72554304
SNPdbers72554304
MSV3drs72554304
GWAS Ctlgrs72554304
Max Magnitude0
ClinVar
Risk rs72554304(T;T)
Alt rs72554304(T;T)
Reference rs72554304(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226560C>T
CLNSRC ClinVar
CLNACC RCV000083618.1,