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rs267608241

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608241(C;T)
Make rs267608241(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position42965712
GenePEX6
is asnp
is mentioned by
dbSNPrs267608241
ebirs267608241
HLIrs267608241
Exacrs267608241
Varsomers267608241
Maprs267608241
PheGenIrs267608241
hapmaprs267608241
1000 genomesrs267608241
hgdprs267608241
ensemblrs267608241
gopubmedrs267608241
geneviewrs267608241
scholarrs267608241
googlers267608241
pharmgkbrs267608241
gwascentralrs267608241
openSNPrs267608241
23andMers267608241
23andMe allrs267608241
SNP Nexus

SNPshotrs267608241
SNPdbers267608241
MSV3drs267608241
GWAS Ctlgrs267608241
Max Magnitude0
ClinVar
Risk rs267608241(T;T)
Alt rs267608241(T;T)
Reference rs267608241(C;C)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 4a (zellweger)
Variation info
Gene PEX6
CLNDBN Peroxisome biogenesis disorder 4a (zellweger)
Reversed 1
HGVS NC_000006.11:g.42933450G>A
CLNSRC
CLNACC RCV000174466.1,