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rs267608176

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608176(-;-)
Make rs267608176(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position92506306
GenePEX1
is asnp
is mentioned by
dbSNPrs267608176
dbSNP (classic)rs267608176
ClinGenrs267608176
ebirs267608176
HLIrs267608176
Exacrs267608176
Gnomadrs267608176
Varsomers267608176
LitVarrs267608176
Maprs267608176
PheGenIrs267608176
Biobankrs267608176
1000 genomesrs267608176
hgdprs267608176
ensemblrs267608176
geneviewrs267608176
scholarrs267608176
googlers267608176
pharmgkbrs267608176
gwascentralrs267608176
openSNPrs267608176
23andMers267608176
23andMe allrs267608176
SNPshotrs267608176
SNPdbers267608176
MSV3drs267608176
GWAS Ctlgrs267608176
Max Magnitude0
ClinVar
Risk rs267608176(-;-)
Alt rs267608176(-;-)
Reference Rs267608176(A;A)
Significance Probable-Pathogenic
Disease Zellweger syndrome Peroxisome biogenesis disorder 1B
Variation info
Gene PEX1
CLNDBN Zellweger syndrome Peroxisome biogenesis disorder 1B
Reversed 1
HGVS NC_000007.13:g.92135620delT
CLNSRC
CLNACC RCV000410765.1, RCV000412291.1,