Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555267839
rs1555267839
T 0.700 GeneticVariation CLINVAR

dbSNP: rs281865022
rs281865022
C 0.700 CausalMutation CLINVAR

dbSNP: rs35333334
rs35333334
A 0.700 CausalMutation CLINVAR When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients. 16630736

2006

dbSNP: rs35333334
rs35333334
A 0.700 CausalMutation CLINVAR Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha beta -subunits precursor gene. 16465621

2006

dbSNP: rs35333334
rs35333334
A 0.700 CausalMutation CLINVAR Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase. 16200072

2005

dbSNP: rs35333334
rs35333334
A 0.700 CausalMutation CLINVAR Mutation Analysis of 16 Mucolipidosis II and III Alpha/Beta Chinese Children Revealed Genotype-Phenotype Correlations. 27662472

2019

dbSNP: rs35333334
rs35333334
A 0.700 CausalMutation CLINVAR Molecular characterization of 22 novel UDP-N-acetylglucosamine-1-phosphate transferase alpha- and beta-subunit (GNPTAB) gene mutations causing mucolipidosis types IIalpha/beta and IIIalpha/beta in 46 patients. 19634183

2009

dbSNP: rs137852900
rs137852900
G 0.800 CausalMutation CLINVAR

dbSNP: rs281864953
rs281864953
A 0.800 CausalMutation CLINVAR

dbSNP: rs281864970
rs281864970
T 0.800 CausalMutation CLINVAR

dbSNP: rs281864970
rs281864970
A 0.800 CausalMutation CLINVAR

dbSNP: rs281865006
rs281865006
G 0.800 CausalMutation CLINVAR

dbSNP: rs281865010
rs281865010
C 0.800 CausalMutation CLINVAR

dbSNP: rs1060499679
rs1060499679
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499680
rs1060499680
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499681
rs1060499681
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499684
rs1060499684
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499685
rs1060499685
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499687
rs1060499687
AT 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499688
rs1060499688
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499689
rs1060499689
A 0.700 GeneticVariation CLINVAR

dbSNP: rs112543062
rs112543062
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1327876395
rs1327876395
A 0.700 GeneticVariation CLINVAR

dbSNP: rs137852895
rs137852895
G 0.700 CausalMutation CLINVAR

dbSNP: rs137852896
rs137852896
A 0.700 CausalMutation CLINVAR