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rs267608188

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TACTT;TACTT) 0 common in clinvar
Make rs267608188(-;-)
Make rs267608188(-;TACTT)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position76983341
GenePEX2
is asnp
is mentioned by
dbSNPrs267608188
dbSNP (old)rs267608188
ClinGenrs267608188
ebirs267608188
HLIrs267608188
Exacrs267608188
Gnomadrs267608188
Varsomers267608188
Maprs267608188
PheGenIrs267608188
Biobankrs267608188
1000 genomesrs267608188
hgdprs267608188
ensemblrs267608188
gopubmedrs267608188
geneviewrs267608188
scholarrs267608188
googlers267608188
pharmgkbrs267608188
gwascentralrs267608188
openSNPrs267608188
23andMers267608188
23andMe allrs267608188
SNPshotrs267608188
SNPdbers267608188
MSV3drs267608188
GWAS Ctlgrs267608188
Max Magnitude0
ClinVar
Risk rs267608188(-;-)
Alt rs267608188(-;-)
Reference Rs267608188(TACTT;TACTT)
Significance Probable-Pathogenic
Disease Peroxisome biogenesis disorder 5B Peroxisome biogenesis disorder 5a (zellweger)
Variation info
Gene PEX2
CLNDBN Peroxisome biogenesis disorder 5B Peroxisome biogenesis disorder 5a (zellweger)
Reversed 1
HGVS NC_000008.10:g.77895577_77895581delAAGTA
CLNSRC
CLNACC RCV000409075.1, RCV000411582.1,