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rs1143016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1143016(C;T)
Make rs1143016(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position2408773
GenePEX10
is asnp
is mentioned by
dbSNPrs1143016
dbSNP (classic)rs1143016
ClinGenrs1143016
ebirs1143016
HLIrs1143016
Exacrs1143016
Gnomadrs1143016
Varsomers1143016
LitVarrs1143016
Maprs1143016
PheGenIrs1143016
Biobankrs1143016
1000 genomesrs1143016
hgdprs1143016
ensemblrs1143016
geneviewrs1143016
scholarrs1143016
googlers1143016
pharmgkbrs1143016
gwascentralrs1143016
openSNPrs1143016
23andMers1143016
SNPshotrs1143016
SNPdbers1143016
MSV3drs1143016
GWAS Ctlgrs1143016
GMAF0.02479
Max Magnitude0
ClinVar
Risk rs1143016(T;T)
Alt rs1143016(T;T)
Reference Rs1143016(C;C)
Significance Other
Disease not specified Zellweger syndrome
Variation info
Gene PEX10
CLNDBN not specified Zellweger syndrome
Reversed 1
HGVS NC_000001.10:g.2340212G>A
CLNSRC Illumina
CLNACC RCV000117901.3, RCV000267822.1,