SLC9A6, solute carrier family 9 member A6, 10479

N. diseases: 210; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122849
rs398122849
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		G 0.700 CausalMutation CLINVAR
dbSNP: rs398123003
rs398123003
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		T 0.700 CausalMutation CLINVAR
dbSNP: rs587784398
rs587784398
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		A 0.700 CausalMutation CLINVAR
dbSNP: rs587784399
rs587784399
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		G 0.700 CausalMutation CLINVAR
dbSNP: rs730882187
rs730882187
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		CC 0.700 CausalMutation CLINVAR
dbSNP: rs730882188
rs730882188
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		C 0.700 CausalMutation CLINVAR
dbSNP: rs796053290
rs796053290
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs796053290
rs796053290
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		C 0.700 CausalMutation CLINVAR
dbSNP: rs796053290
rs796053290
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0025362
Disease:
Mental Retardation 		C 0.700 CausalMutation CLINVAR
dbSNP: rs886037619
rs886037619
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		G 0.700 CausalMutation CLINVAR
dbSNP: rs398124224
rs398124224
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type 		0.010 GeneticVariation BEFREE We report on a 22year-old male patient with Christianson syndrome carrying the novel p.Gln306X mutation. 22541666 2013