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rs104893661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893661(A;A)
Make rs104893661(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position61032028
GenePEX13
is asnp
is mentioned by
dbSNPrs104893661
ebirs104893661
HLIrs104893661
Exacrs104893661
Varsomers104893661
Maprs104893661
PheGenIrs104893661
hapmaprs104893661
1000 genomesrs104893661
hgdprs104893661
ensemblrs104893661
gopubmedrs104893661
geneviewrs104893661
scholarrs104893661
googlers104893661
pharmgkbrs104893661
gwascentralrs104893661
openSNPrs104893661
23andMers104893661
23andMe allrs104893661
SNP Nexus

SNPshotrs104893661
SNPdbers104893661
MSV3drs104893661
GWAS Ctlgrs104893661
Max Magnitude0
OMIM601789
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893661(A;A)
Alt rs104893661(A;A)
Reference rs104893661(G;G)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 11A
Variation info
Gene PEX13
CLNDBN Peroxisome biogenesis disorder 11A
Reversed 0
HGVS NC_000002.11:g.61259163G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008142.2,