rs1515751
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
Atrial Fibrillation
0.010
GeneticVariation
BEFREE
Moreover, the A allele of rs1515751 had a significant association with AF onset.
31406021
2019
rs1515752
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
Hypertensive disease
0.010
GeneticVariation
BEFREE
The prevalence of hypertension was associated with rs1515752 , and left atrial size was associated with the genotype of rs2071438.
31406021
2019
rs2071438
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
Hypertensive disease
0.010
GeneticVariation
BEFREE
The prevalence of hypertension was associated with rs1515752, and left atrial size was associated with the genotype of rs2071438 .
31406021
2019
rs4968309
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
Diabetes Mellitus
0.010
GeneticVariation
BEFREE
C allele and CC genotype of rs4968309 and A allele of rs1515751were associated with AF onset both before and after adjustment of covariation (age, sex, hypertension, and diabetes ).
31406021
2019
rs4968309
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
Diabetes
0.010
GeneticVariation
BEFREE
C allele and CC genotype of rs4968309 and A allele of rs1515751were associated with AF onset both before and after adjustment of covariation (age, sex, hypertension, and diabetes ).
31406021
2019
rs4968309
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
Atrial Fibrillation
0.010
GeneticVariation
BEFREE
C allele and CC genotype of rs4968309 inMYL4were associated with AF onset and recurrence.
31406021
2019
rs886037778
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
ATRIAL FIBRILLATION, FAMILIAL, 18
0.700
GeneticVariation
UNIPROT
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.
27066836
2016
rs886037778
×
Entrez Id:
4635
Gene Symbol:
MYL4
MYL4
familial atrial fibrillation
A
0.700
CausalMutation
CLINVAR
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.
27066836
2016