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rs72556302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556302(A;A)
Make rs72556302(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403667
GeneOTC
is asnp
is mentioned by
dbSNPrs72556302
dbSNP (classic)rs72556302
ClinGenrs72556302
ebirs72556302
HLIrs72556302
Exacrs72556302
Gnomadrs72556302
Varsomers72556302
LitVarrs72556302
Maprs72556302
PheGenIrs72556302
Biobankrs72556302
1000 genomesrs72556302
hgdprs72556302
ensemblrs72556302
geneviewrs72556302
scholarrs72556302
googlers72556302
pharmgkbrs72556302
gwascentralrs72556302
openSNPrs72556302
23andMers72556302
SNPshotrs72556302
SNPdbers72556302
MSV3drs72556302
GWAS Ctlgrs72556302
Max Magnitude0
ClinVar
Risk rs72556302(A;A)
Alt rs72556302(A;A)
Reference Rs72556302(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262920G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000083503.1,