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: rs121913636
rs121913636
MYH7
2 0.925 0.080 14 23428540 missense variant A/C snv 0.800 1.000 25 1992 2017
dbSNP: rs730880735
rs730880735
MYH7
1 1.000 0.080 14 23425417 missense variant A/C snv 0.700 0
dbSNP: rs727505202
rs727505202
MYH7
1 1.000 0.080 14 23431459 missense variant A/C;G snv 0.700 0
dbSNP: rs397516157
rs397516157
MYH7
3 0.882 0.080 14 23424893 missense variant A/C;G;T snv 4.0E-06 0.800 1.000 25 1992 2017
dbSNP: rs863224900
rs863224900
MYH7
6 0.807 0.160 14 23428534 missense variant A/C;G;T snv 0.700 0
dbSNP: rs397516269
rs397516269
MYH7
4 0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 0.800 1.000 28 1992 2017
dbSNP: rs397516110
rs397516110
MYH7
1 1.000 0.080 14 23428546 missense variant A/G snv 0.800 1.000 25 1992 2017
dbSNP: rs397516130
rs397516130
MYH7
3 0.882 0.080 14 23426033 missense variant A/G snv 0.800 1.000 21 1992 2005
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: rs397516183
rs397516183
MYH7
2 0.925 0.080 14 23433086 missense variant A/G snv 4.0E-06 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: rs730880849
rs730880849
MYH7
1 1.000 0.080 14 23431587 missense variant A/G snv 0.700 0
dbSNP: rs727503261
rs727503261
MYH7
3 0.882 0.080 14 23425774 missense variant A/G;T snv 0.800 1.000 19 2003 2017
dbSNP: rs397516087
rs397516087
MYH7
1 1.000 0.080 14 23429900 missense variant A/G;T snv 0.700 0
dbSNP: rs863225095
rs863225095
MYH7
1 1.000 0.080 14 23424793 missense variant A/T snv 7.0E-06 0.700 0
dbSNP: rs863225102
rs863225102
MYH7
1 1.000 0.080 14 23425414 missense variant A/T snv 0.700 0
dbSNP: rs267606911
rs267606911
MYH7
3 0.882 0.080 14 23428587 missense variant C/A snv 8.0E-06 0.800 1.000 20 1992 2005
dbSNP: rs397516095
rs397516095
MYH7
2 0.925 0.080 14 23429266 missense variant C/A snv 0.700 1.000 20 1992 2005
dbSNP: rs772691929
rs772691929
MYH7
1 1.000 0.080 14 23432698 missense variant C/A snv 4.0E-06 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: rs36211715
rs36211715
MYH7
5 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 39 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: rs3218716
rs3218716
MYH7
17 0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 0.800 1.000 32 1975 2017
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: 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