Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113382956
rs113382956
Entrez Id: 8208;23515
Gene Symbol: CHAF1B;MORC3
CHAF1B;MORC3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs113382956
rs113382956
Entrez Id: 8208;23515
Gene Symbol: CHAF1B;MORC3
CHAF1B;MORC3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs170144
rs170144
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs73204208
rs73204208
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs75530000
rs75530000
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs140630794
rs140630794
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B
CUI: C0557874
Disease:
Global developmental delay 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs140630794
rs140630794
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs140630794
rs140630794
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B
CUI: C1843367
Disease:
Poor school performance 		G 0.700 GeneticVariation CLINVAR