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rs1057523689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523689(A;A)
Make rs1057523689(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position143485201
GenePEX3
is asnp
is mentioned by
dbSNPrs1057523689
dbSNP (old)rs1057523689
ClinGenrs1057523689
ebirs1057523689
HLIrs1057523689
Exacrs1057523689
Gnomadrs1057523689
Varsomers1057523689
LitVarrs1057523689
Maprs1057523689
PheGenIrs1057523689
Biobankrs1057523689
1000 genomesrs1057523689
hgdprs1057523689
ensemblrs1057523689
gopubmedrs1057523689
geneviewrs1057523689
scholarrs1057523689
googlers1057523689
pharmgkbrs1057523689
gwascentralrs1057523689
openSNPrs1057523689
23andMers1057523689
23andMe allrs1057523689
SNPshotrs1057523689
SNPdbers1057523689
MSV3drs1057523689
GWAS Ctlgrs1057523689
Max Magnitude0
ClinVar
Risk rs1057523689(A;A)
Alt rs1057523689(A;A)
Reference Rs1057523689(G;G)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 10b
Variation info
Gene PEX3
CLNDBN Peroxisome biogenesis disorder 10b
Reversed 0
HGVS NC_000006.11:g.143806338G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000433323.1,