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rs61752094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752094(C;G)
Make rs61752094(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position2406528
GenePEX10
is asnp
is mentioned by
dbSNPrs61752094
ebirs61752094
HLIrs61752094
Exacrs61752094
Varsomers61752094
Maprs61752094
PheGenIrs61752094
hapmaprs61752094
1000 genomesrs61752094
hgdprs61752094
ensemblrs61752094
gopubmedrs61752094
geneviewrs61752094
scholarrs61752094
googlers61752094
pharmgkbrs61752094
gwascentralrs61752094
openSNPrs61752094
23andMers61752094
23andMe allrs61752094
SNP Nexus

SNPshotrs61752094
SNPdbers61752094
MSV3drs61752094
GWAS Ctlgrs61752094
Max Magnitude0

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


ClinVar
Risk rs61752094(G;G)
Alt rs61752094(G;G)
Reference rs61752094(C;C)
Significance Untested
Disease
Variation info
Gene PEX10
CLNDBN
Reversed 1
HGVS NC_000001.10:g.2337967G>C
CLNSRC
CLNACC