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rs797044762

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044762(-;G)
Make rs797044762(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position2406528
GenePEX10
is asnp
is mentioned by
dbSNPrs797044762
ClinGenrs797044762
ebirs797044762
HLIrs797044762
Exacrs797044762
Varsomers797044762
Maprs797044762
PheGenIrs797044762
hapmaprs797044762
1000 genomesrs797044762
hgdprs797044762
ensemblrs797044762
gopubmedrs797044762
geneviewrs797044762
scholarrs797044762
googlers797044762
pharmgkbrs797044762
gwascentralrs797044762
openSNPrs797044762
23andMers797044762
23andMe allrs797044762
SNP Nexus

SNPshotrs797044762
SNPdbers797044762
MSV3drs797044762
GWAS Ctlgrs797044762
Max Magnitude0
ClinVar
Risk rs797044762(G;G)
Alt rs797044762(G;G)
Reference Rs797044762(;)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 6A
Variation info
Gene PEX10
CLNDBN Peroxisome biogenesis disorder 6A
Reversed 1
HGVS NC_000001.10:g.2337967_2337968insC
CLNSRC
CLNACC RCV000179026.1,