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rs387906809

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906809(C;C)
Make rs387906809(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position42968377
GenePEX6
is asnp
is mentioned by
dbSNPrs387906809
ebirs387906809
HLIrs387906809
Exacrs387906809
Varsomers387906809
Maprs387906809
PheGenIrs387906809
hapmaprs387906809
1000 genomesrs387906809
hgdprs387906809
ensemblrs387906809
gopubmedrs387906809
geneviewrs387906809
scholarrs387906809
googlers387906809
pharmgkbrs387906809
gwascentralrs387906809
openSNPrs387906809
23andMers387906809
23andMe allrs387906809
SNP Nexus

SNPshotrs387906809
SNPdbers387906809
MSV3drs387906809
GWAS Ctlgrs387906809
Max Magnitude0
ClinVar
Risk rs387906809(C;C)
Alt rs387906809(C;C)
Reference rs387906809(T;T)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 4B
Variation info
Gene PEX6
CLNDBN Peroxisome biogenesis disorder 4B
Reversed 1
HGVS NC_000006.11:g.42936115A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023114.5,