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rs797045062

From SNPedia

Orientationminus
Make rs797045062(-;-)
Make rs797045062(-;TCT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position45910268
GenePEX16
is asnp
is mentioned by
dbSNPrs797045062
ebirs797045062
HLIrs797045062
Exacrs797045062
Varsomers797045062
Maprs797045062
PheGenIrs797045062
hapmaprs797045062
1000 genomesrs797045062
hgdprs797045062
ensemblrs797045062
gopubmedrs797045062
geneviewrs797045062
scholarrs797045062
googlers797045062
pharmgkbrs797045062
gwascentralrs797045062
openSNPrs797045062
23andMers797045062
23andMe allrs797045062
SNP Nexus

SNPshotrs797045062
SNPdbers797045062
MSV3drs797045062
GWAS Ctlgrs797045062
Max Magnitude
ClinVar
Risk rs797045062(;)
Alt rs797045062(;)
Reference rs797045062(TCT;TCT)
Significance Probable-Pathogenic
Disease Peroxisome biogenesis disorder 8B
Variation info
Gene PEX16
CLNDBN Peroxisome biogenesis disorder 8B
Reversed 1
HGVS NC_000011.9:g.45931819_45931821delAGA
CLNSRC Baylor College of Medicine
CLNACC RCV000191117.1,