DYNLL1, dynein light chain LC8-type 1, 8655

N. diseases: 103; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17431717
rs17431717
Entrez Id: 8655
Gene Symbol: DYNLL1
DYNLL1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs17431717
rs17431717
Entrez Id: 8655
Gene Symbol: DYNLL1
DYNLL1
CUI: C0596887
Disease:
mathematical ability 		G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs11352199
rs11352199
Entrez Id: 8655
Gene Symbol: DYNLL1
DYNLL1
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4767902
rs4767902
Entrez Id: 8655
Gene Symbol: DYNLL1
DYNLL1
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs558163981
rs558163981
Entrez Id: 8655
Gene Symbol: DYNLL1
DYNLL1
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		CA 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10849753
rs10849753
Entrez Id: 8655
Gene Symbol: DYNLL1
DYNLL1
CUI: C1847540
Disease:
Azoospermia, Nonobstructive 		0.010 GeneticVariation BEFREE Rs17431717 near SFRS9 and rs12046213 near SFRS4 were significantly associated with a decreased risk of NOA, whereas rs10849753 near SFRS9 and rs6103330 in SFRS6 were associated with an increased risk of NOA. 24661730 2014