Gene: ZSWIM6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		0.120 GeneticVariation disease BEFREE Additionally, a putatively causal point mutation in ZSWIM6 has been identified in several cases of acromelic frontonasal dysostosis with severe intellectual disability. 28433741 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		0.120 CausalMutation disease CLINVAR A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations. 29198722 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		0.120 GeneticVariation disease BEFREE A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations. 29198722 2017