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rs724160029

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs724160029(-;-)
Make rs724160029(-;A)
Make rs724160029(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position76983313
GenePEX2
is asnp
is mentioned by
dbSNPrs724160029
ebirs724160029
HLIrs724160029
Exacrs724160029
Varsomers724160029
Maprs724160029
PheGenIrs724160029
hapmaprs724160029
1000 genomesrs724160029
hgdprs724160029
ensemblrs724160029
gopubmedrs724160029
geneviewrs724160029
scholarrs724160029
googlers724160029
pharmgkbrs724160029
gwascentralrs724160029
openSNPrs724160029
23andMers724160029
23andMe allrs724160029
SNP Nexus

SNPshotrs724160029
SNPdbers724160029
MSV3drs724160029
GWAS Ctlgrs724160029
Max Magnitude0
ClinVar
Risk rs724160029(A;A)
Alt rs724160029(A;A)
Reference rs724160029(;)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 5B
Variation info
Gene PEX2
CLNDBN Peroxisome biogenesis disorder 5B
Reversed 1
HGVS NC_000008.10:g.77895550dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000149879.3,