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rs62636524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62636524(-;-)
Make rs62636524(-;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position2412499
GenePEX10
is asnp
is mentioned by
dbSNPrs62636524
ebirs62636524
HLIrs62636524
Exacrs62636524
Varsomers62636524
Maprs62636524
PheGenIrs62636524
hapmaprs62636524
1000 genomesrs62636524
hgdprs62636524
ensemblrs62636524
gopubmedrs62636524
geneviewrs62636524
scholarrs62636524
googlers62636524
pharmgkbrs62636524
gwascentralrs62636524
openSNPrs62636524
23andMers62636524
23andMe allrs62636524
SNP Nexus

SNPshotrs62636524
SNPdbers62636524
MSV3drs62636524
GWAS Ctlgrs62636524
Max Magnitude0
ClinVar
Risk rs62636524(;)
Alt rs62636524(;)
Reference rs62636524(G;G)
Significance Untested
Disease
Variation info
Gene PEX10
CLNDBN
Reversed 1
HGVS NC_000001.10:g.2343938delC
CLNSRC
CLNACC


[PMID 15542397] The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.