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rs72558447

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558447(A;A)
Make rs72558447(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408953
GeneOTC
is asnp
is mentioned by
dbSNPrs72558447
ebirs72558447
HLIrs72558447
Exacrs72558447
Varsomers72558447
Maprs72558447
PheGenIrs72558447
hapmaprs72558447
1000 genomesrs72558447
hgdprs72558447
ensemblrs72558447
gopubmedrs72558447
geneviewrs72558447
scholarrs72558447
googlers72558447
pharmgkbrs72558447
gwascentralrs72558447
openSNPrs72558447
23andMers72558447
23andMe allrs72558447
SNP Nexus

SNPshotrs72558447
SNPdbers72558447
MSV3drs72558447
GWAS Ctlgrs72558447
Max Magnitude0
ClinVar
Risk rs72558447(A;A)
Alt rs72558447(A;A)
Reference rs72558447(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268206G>A
CLNSRC ClinVar
CLNACC RCV000083578.1,