Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518957
rs1057518957
CHRND
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518958
rs1057518958
CHRND
CUI: C0013404
Disease: Dyspnea
Dyspnea 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519439
rs1057519439
DNAH7
CUI: C0013404
Disease: Dyspnea
Dyspnea 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1163944538
rs1163944538
TMEM94
CUI: C0013404
Disease: Dyspnea
Dyspnea 		GA 0.700 CausalMutation CLINVAR

dbSNP: rs1178187217
rs1178187217
DNAH11
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs121918459
rs121918459
PTPN11
CUI: C0013404
Disease: Dyspnea
Dyspnea 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1294950721
rs1294950721
JAG1
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
CUI: C0013404
Disease: Dyspnea
Dyspnea 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1553621496
rs1553621496
UNC80
CUI: C0013404
Disease: Dyspnea
Dyspnea 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1569548274
rs1569548274
MECP2
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 CausalMutation CLINVAR

dbSNP: rs201943194
rs201943194
DNAH11
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
FKRP
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 CausalMutation CLINVAR

dbSNP: rs397514698
rs397514698
GNAQ
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 CausalMutation CLINVAR

dbSNP: rs543860009
rs543860009
TTN ; TTN-AS1
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 CausalMutation CLINVAR

dbSNP: rs587782958
rs587782958
MYBPC3
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 CausalMutation CLINVAR

dbSNP: rs727505026
rs727505026
MYH7 ; MIR208B
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs759191907
rs759191907
ENG ; LOC105379841
CUI: C0013404
Disease: Dyspnea
Dyspnea 		G 0.700 CausalMutation CLINVAR

dbSNP: rs780533096
rs780533096
MIPEP
CUI: C0013404
Disease: Dyspnea
Dyspnea 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs796051877
rs796051877
GAA
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 CausalMutation CLINVAR c.1437G>A intron 9 substitution on acid α-glucosidase gene associated with classic infantile-onset Pompe disease phenotype. 26160551

2015
dbSNP: rs878854378
rs878854378
TTN ; TTN-AS1
CUI: C0013404
Disease: Dyspnea
Dyspnea 		A 0.700 GeneticVariation CLINVAR