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rs267608179

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608179(A;A)
Make rs267608179(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position92494486
GenePEX1
is asnp
is mentioned by
dbSNPrs267608179
ebirs267608179
HLIrs267608179
Exacrs267608179
Varsomers267608179
Maprs267608179
PheGenIrs267608179
hapmaprs267608179
1000 genomesrs267608179
hgdprs267608179
ensemblrs267608179
gopubmedrs267608179
geneviewrs267608179
scholarrs267608179
googlers267608179
pharmgkbrs267608179
gwascentralrs267608179
openSNPrs267608179
23andMers267608179
23andMe allrs267608179
SNP Nexus

SNPshotrs267608179
SNPdbers267608179
MSV3drs267608179
GWAS Ctlgrs267608179
Max Magnitude0
ClinVar
Risk rs267608179(A;A)
Alt rs267608179(A;A)
Reference rs267608179(G;G)
Significance Probable-Pathogenic
Disease Zellweger syndrome
Variation info
Gene PEX1
CLNDBN Zellweger syndrome
Reversed 1
HGVS NC_000007.13:g.92123800C>T
CLNSRC
CLNACC RCV000169032.1,