Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113809617
rs113809617
Entrez Id: 27158;94107
Gene Symbol: NDOR1;TMEM203
NDOR1;TMEM203
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs113809617
rs113809617
Entrez Id: 27158;94107
Gene Symbol: NDOR1;TMEM203
NDOR1;TMEM203
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs28404308
rs28404308
Entrez Id: 27158
Gene Symbol: NDOR1
NDOR1
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs113809617
rs113809617
Entrez Id: 27158;94107
Gene Symbol: NDOR1;TMEM203
NDOR1;TMEM203
CUI: C0524587
Disease:
Mean Corpuscular Volume (result)
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs113809617
rs113809617
Entrez Id: 27158;94107
Gene Symbol: NDOR1;TMEM203
NDOR1;TMEM203
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs113809617
rs113809617
Entrez Id: 27158;94107
Gene Symbol: NDOR1;TMEM203
NDOR1;TMEM203
CUI: C0206161
Disease:
Reticulocyte count (procedure)
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs113809617
rs113809617
Entrez Id: 27158;94107
Gene Symbol: NDOR1;TMEM203
NDOR1;TMEM203
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016