HOXD10, homeobox D10, 3236

N. diseases: 83; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893634
rs104893634
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C0240912
Disease:
Vertical Talus 		0.810 GeneticVariation BEFREE HOXD10 M319K mutation in a family with isolated congenital vertical talus. 16450407 2006
dbSNP: rs104893634
rs104893634
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C0240912
Disease:
Vertical Talus 		0.810 GeneticVariation UNIPROT A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease. 15146389 2004
dbSNP: rs104893634
rs104893634
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C0240912
Disease:
Vertical Talus 		A 0.810 CausalMutation CLINVAR
dbSNP: rs863678
rs863678
Entrez Id: 3236;3237
Gene Symbol: HOXD10;HOXD11
HOXD10;HOXD11
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs863678
rs863678
Entrez Id: 3236;3237
Gene Symbol: HOXD10;HOXD11
HOXD10;HOXD11
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		T 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs863678
rs863678
Entrez Id: 3236;3237
Gene Symbol: HOXD10;HOXD11
HOXD10;HOXD11
CUI: C0018935
Disease:
Hematocrit procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7601234
rs7601234
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C3542025
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs7601234
rs7601234
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C1862941
Disease:
Amyotrophic Lateral Sclerosis, Sporadic 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs7601234
rs7601234
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs7601234
rs7601234
Entrez Id: 3236
Gene Symbol: HOXD10
HOXD10
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014