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rs267608190

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608190(G;T)
Make rs267608190(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position18078607
GenePEX26
is asnp
is mentioned by
dbSNPrs267608190
ebirs267608190
HLIrs267608190
Exacrs267608190
Varsomers267608190
Maprs267608190
PheGenIrs267608190
hapmaprs267608190
1000 genomesrs267608190
hgdprs267608190
ensemblrs267608190
gopubmedrs267608190
geneviewrs267608190
scholarrs267608190
googlers267608190
pharmgkbrs267608190
gwascentralrs267608190
openSNPrs267608190
23andMers267608190
23andMe allrs267608190
SNP Nexus

SNPshotrs267608190
SNPdbers267608190
MSV3drs267608190
GWAS Ctlgrs267608190
Max Magnitude0
ClinVar
Risk rs267608190(T;T)
Alt rs267608190(T;T)
Reference rs267608190(G;G)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 7A
Variation info
Gene PEX26
CLNDBN Peroxisome biogenesis disorder 7A
Reversed 0
HGVS NC_000022.10:g.18561373G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002242.2,