Gene: MYH7 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057517771
rs1057517771
MYH7
1 1.000 0.080 14 23432656 missense variant T/C snv 0.700 0
dbSNP: rs1057517772
rs1057517772
MYH7
1 1.000 0.080 14 23431839 missense variant G/A;C snv 0.700 0
dbSNP: rs121913624
rs121913624
MYH7
4 0.851 0.080 14 23429278 missense variant C/A;G;T snv 0.800 1.000 76 1961 2017
dbSNP: rs121913625
rs121913625
MYH7
4 0.851 0.080 14 23429005 missense variant G/A;C;T snv 0.800 1.000 34 1990 2014
dbSNP: rs121913626
rs121913626
MYH7
3 0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 26 1992 2014
dbSNP: rs121913627
rs121913627
MYH7
8 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 30 1992 2014
dbSNP: rs121913628
rs121913628
MYH7
10 0.763 0.160 14 23424059 missense variant C/G;T snv 0.800 1.000 34 1992 2017
dbSNP: rs121913629
rs121913629
MYH7
1 1.000 0.080 14 23423984 missense variant C/T snv 0.700 1.000 25 1992 2017
dbSNP: rs121913630
rs121913630
MYH7
7 0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 0.800 1.000 35 1992 2017
dbSNP: rs121913631
rs121913631
MYH7
3 0.882 0.080 14 23424107 missense variant G/C snv 1.4E-05 0.800 1.000 37 1992 2017
dbSNP: rs121913632
rs121913632
MYH7
3 0.882 0.080 14 23425760 missense variant C/A;G;T snv 0.800 1.000 33 1992 2017
dbSNP: rs121913633
rs121913633
MYH7
3 0.882 0.080 14 23431447 missense variant C/T snv 7.0E-06 0.800 1.000 20 1992 2005
dbSNP: rs121913634
rs121913634
MYH7
3 0.882 0.080 14 23425372 missense variant T/A;C snv 0.800 1.000 25 1992 2017
dbSNP: rs121913636
rs121913636
MYH7
2 0.925 0.080 14 23428540 missense variant A/C snv 0.800 1.000 25 1992 2017
dbSNP: rs121913637
rs121913637
MYH7
3 0.882 0.080 14 23425971 missense variant G/A snv 7.0E-06 0.800 1.000 50 1992 2017
dbSNP: rs121913638
rs121913638
MYH7
4 0.851 0.120 14 23425980 missense variant C/T snv 0.800 1.000 22 1992 2005
dbSNP: rs121913639
rs121913639
MYH7
1 1.000 0.080 14 23424026 missense variant C/T snv 0.800 1.000 25 1992 2017
dbSNP: rs121913640
rs121913640
MYH7
1 1.000 0.080 14 23429867 missense variant A/G snv 2.1E-05 0.700 1.000 20 1992 2005
dbSNP: rs121913641
rs121913641
MYH7
3 0.882 0.080 14 23425970 missense variant C/G;T snv 0.800 1.000 35 1992 2017
dbSNP: rs121913644
rs121913644
MYH7
1 1.000 0.080 14 23425798 missense variant G/A snv 1.6E-04 9.1E-05 0.700 1.000 20 1992 2005
dbSNP: rs121913650
rs121913650
MYH7 ; MHRT
2 0.925 0.080 14 23415652 missense variant G/A snv 7.0E-06 0.800 1.000 20 1992 2005
dbSNP: rs121913651
rs121913651
MYH7
2 0.925 0.080 14 23428631 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 25 1992 2017
dbSNP: rs121913652
rs121913652
MYH7 ; MHRT
3 0.882 0.080 14 23414015 missense variant C/T snv 7.0E-06 0.700 1.000 20 1992 2005
dbSNP: rs121913654
rs121913654
MYH7 ; MHRT
3 0.882 0.160 14 23415176 missense variant A/G snv 0.700 0
dbSNP: rs141764279
rs141764279
MYH7 ; MIR208B
1 1.000 0.080 14 23418398 missense variant G/A;T snv 2.8E-05; 1.1E-04 0.700 1.000 27 1992 2017