Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability. 25281490

2015
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR Refining analyses of copy number variation identifies specific genes associated with developmental delay. 25217958

2014
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR ZMYND11: an H3.3-specific reader of H3K36me3. 24963723

2014
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression. 24590075

2014
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR Structural and functional analysis of the DEAF-1 and BS69 MYND domains. 23372760

2013
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886

2013
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization. 22847950

2012
dbSNP: rs797044854
rs797044854
ZMYND11
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		T 0.700 CausalMutation CLINVAR New insights into BS69 functions. 16565076

2006