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rs149806989

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149806989(A;A)
Make rs149806989(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position92517968
GenePEX1
is asnp
is mentioned by
dbSNPrs149806989
dbSNP (classic)rs149806989
ClinGenrs149806989
ebirs149806989
HLIrs149806989
Exacrs149806989
Gnomadrs149806989
Varsomers149806989
LitVarrs149806989
Maprs149806989
PheGenIrs149806989
Biobankrs149806989
1000 genomesrs149806989
hgdprs149806989
ensemblrs149806989
geneviewrs149806989
scholarrs149806989
googlers149806989
pharmgkbrs149806989
gwascentralrs149806989
openSNPrs149806989
23andMers149806989
23andMe allrs149806989
SNPshotrs149806989
SNPdbers149806989
MSV3drs149806989
GWAS Ctlgrs149806989
Max Magnitude0
ClinVar
Risk rs149806989(A;A)
Alt rs149806989(A;A)
Reference Rs149806989(G;G)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 1B Zellweger syndrome
Variation info
Gene PEX1
CLNDBN Peroxisome biogenesis disorder 1B Zellweger syndrome
Reversed 0
HGVS NC_000007.13:g.92147282G>A
CLNSRC
CLNACC RCV000409397.1, RCV000411910.1,