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rs61752096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61752096(A;A)
Make rs61752096(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position2406515
GenePEX10
is asnp
is mentioned by
dbSNPrs61752096
ebirs61752096
HLIrs61752096
Exacrs61752096
Varsomers61752096
Maprs61752096
PheGenIrs61752096
hapmaprs61752096
1000 genomesrs61752096
hgdprs61752096
ensemblrs61752096
gopubmedrs61752096
geneviewrs61752096
scholarrs61752096
googlers61752096
pharmgkbrs61752096
gwascentralrs61752096
openSNPrs61752096
23andMers61752096
23andMe allrs61752096
SNP Nexus

SNPshotrs61752096
SNPdbers61752096
MSV3drs61752096
GWAS Ctlgrs61752096
Max Magnitude0

[PMID 17041890] Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.


ClinVar
Risk rs61752096(A;A)
Alt rs61752096(A;A)
Reference rs61752096(G;G)
Significance Untested
Disease
Variation info
Gene PEX10
CLNDBN
Reversed 1
HGVS NC_000001.10:g.2337954C>T
CLNSRC
CLNACC