Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10947055
rs10947055 		0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs12757165
rs12757165
ESRRG
0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs12907914
rs12907914
LINC02694 ; LOC105370781
0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs1320448
rs1320448
COL17A1
0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs1484170
rs1484170 		0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs152528
rs152528
FGF1 ; SPRY4-AS1
0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs16830359
rs16830359 		0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs17636733
rs17636733 		0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs1916521
rs1916521 		0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs3729931
rs3729931
RAF1
0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951

2011
dbSNP: rs80338796
rs80338796
RAF1
A 0.700 CausalMutation CLINVAR Germline gain-of-function mutations in RAF1 cause Noonan syndrome. 17603482

2007
dbSNP: rs80338796
rs80338796
RAF1
A 0.700 CausalMutation CLINVAR Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. 17603483

2007