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rs724160000

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs724160000(C;C)
Make rs724160000(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position2406566
GenePEX10
is asnp
is mentioned by
dbSNPrs724160000
ebirs724160000
HLIrs724160000
Exacrs724160000
Varsomers724160000
Maprs724160000
PheGenIrs724160000
hapmaprs724160000
1000 genomesrs724160000
hgdprs724160000
ensemblrs724160000
gopubmedrs724160000
geneviewrs724160000
scholarrs724160000
googlers724160000
pharmgkbrs724160000
gwascentralrs724160000
openSNPrs724160000
23andMers724160000
23andMe allrs724160000
SNP Nexus

SNPshotrs724160000
SNPdbers724160000
MSV3drs724160000
GWAS Ctlgrs724160000
Max Magnitude0
ClinVar
Risk rs724160000(C;C)
Alt rs724160000(C;C)
Reference rs724160000(T;T)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 6B
Variation info
Gene PEX10
CLNDBN Peroxisome biogenesis disorder 6B
Reversed 1
HGVS NC_000001.10:g.2338005A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149810.4,