KANSL1, KAT8 regulatory NSL complex subunit 1, 284058

N. diseases: 140; N. variants: 332
Disease: Multiple congenital anomalies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555574888
rs1555574888
Entrez Id: 284058
Gene Symbol: KANSL1
KANSL1
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 CausalMutation CLINVAR The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant. 26306646 2016
dbSNP: rs1555574888
rs1555574888
Entrez Id: 284058
Gene Symbol: KANSL1
KANSL1
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 CausalMutation CLINVAR KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome. 26293599 2015
dbSNP: rs1555574888
rs1555574888
Entrez Id: 284058
Gene Symbol: KANSL1
KANSL1
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 CausalMutation CLINVAR Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. 26424144 2015
dbSNP: rs1555574888
rs1555574888
Entrez Id: 284058
Gene Symbol: KANSL1
KANSL1
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 CausalMutation CLINVAR Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. 22544363 2012
dbSNP: rs1555574888
rs1555574888
Entrez Id: 284058
Gene Symbol: KANSL1
KANSL1
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 CausalMutation CLINVAR Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype. 22544367 2012