Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs606231456
rs606231456
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		0.800 GeneticVariation UNIPROT NDST1 missense mutations in autosomal recessive intellectual disability. 25125150 2014
dbSNP: rs606231457
rs606231457
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		0.800 GeneticVariation UNIPROT NDST1 missense mutations in autosomal recessive intellectual disability. 25125150 2014
dbSNP: rs606231458
rs606231458
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		0.800 GeneticVariation UNIPROT NDST1 missense mutations in autosomal recessive intellectual disability. 25125150 2014
dbSNP: rs606231459
rs606231459
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		0.800 GeneticVariation UNIPROT NDST1 missense mutations in autosomal recessive intellectual disability. 25125150 2014
dbSNP: rs606231456
rs606231456
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		A 0.800 CausalMutation CLINVAR
dbSNP: rs606231457
rs606231457
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		T 0.800 CausalMutation CLINVAR
dbSNP: rs606231458
rs606231458
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		C 0.800 CausalMutation CLINVAR
dbSNP: rs606231459
rs606231459
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C4015283
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 		A 0.800 CausalMutation CLINVAR
dbSNP: rs17726577
rs17726577
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2545339
rs2545339
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3846706
rs3846706
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2545342
rs2545342
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C0027051
Disease:
Myocardial Infarction 		0.700 GeneticVariation GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
dbSNP: rs2273235
rs2273235
Entrez Id: 3340
Gene Symbol: NDST1
NDST1
CUI: C1531624
Disease:
Cardioembolic stroke 		0.010 GeneticVariation BEFREE Similar results were found for m<sup>6</sup>A-SNP rs2273235 in the <i>NDST1</i> gene which was associated with cardioembolic stroke (<i>P</i> = 8.47 × 10<sup>-3</sup>). 31156544 2019