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rs72556285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACGCTC;ACGCTC) 0 common in clinvar
(CTCACG;CTCACG) 0 common in clinvar
(I;I) 0
Make rs72556285(-;-)
Make rs72556285(-;ACGCTC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401420
GeneOTC
is asnp
is mentioned by
dbSNPrs72556285
ebirs72556285
HLIrs72556285
Exacrs72556285
Varsomers72556285
Maprs72556285
PheGenIrs72556285
hapmaprs72556285
1000 genomesrs72556285
hgdprs72556285
ensemblrs72556285
gopubmedrs72556285
geneviewrs72556285
scholarrs72556285
googlers72556285
pharmgkbrs72556285
gwascentralrs72556285
openSNPrs72556285
23andMers72556285
23andMe allrs72556285
SNP Nexus

SNPshotrs72556285
SNPdbers72556285
MSV3drs72556285
GWAS Ctlgrs72556285
Max Magnitude0
ClinVar
Risk rs72556285(;)
Alt rs72556285(;)
Reference rs72556285(CTCACG;CTCACG)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260673_38260678delACGCTC
CLNSRC ClinVar
CLNACC RCV000083476.1,