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rs72556256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556256(A;A)
Make rs72556256(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401292
GeneOTC
is asnp
is mentioned by
dbSNPrs72556256
ebirs72556256
HLIrs72556256
Exacrs72556256
Varsomers72556256
Maprs72556256
PheGenIrs72556256
hapmaprs72556256
1000 genomesrs72556256
hgdprs72556256
ensemblrs72556256
gopubmedrs72556256
geneviewrs72556256
scholarrs72556256
googlers72556256
pharmgkbrs72556256
gwascentralrs72556256
openSNPrs72556256
23andMers72556256
23andMe allrs72556256
SNP Nexus

SNPshotrs72556256
SNPdbers72556256
MSV3drs72556256
GWAS Ctlgrs72556256
Max Magnitude0
ClinVar
Risk rs72556256(A;A)
Alt rs72556256(A;A)
Reference rs72556256(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260545C>A
CLNSRC ClinVar
CLNACC RCV000083426.1,