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: rs121913625
rs121913625
MYH7
4 0.851 0.080 14 23429005 missense variant G/A;C;T snv 0.700 1.000 19 1992 2014
dbSNP: rs121913632
rs121913632
MYH7
3 0.882 0.080 14 23425760 missense variant C/A;G;T snv 0.700 1.000 19 1985 2017
dbSNP: rs121913626
rs121913626
MYH7
3 0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 17 1992 2018
dbSNP: rs36211715
rs36211715
MYH7
5 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 16 1995 2017
dbSNP: rs121913627
rs121913627
MYH7
8 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 15 1992 2014
dbSNP: rs121913624
rs121913624
MYH7
4 0.851 0.080 14 23429278 missense variant C/A;G;T snv 0.710 1.000 14 1990 2018
dbSNP: rs397516127
rs397516127
MYH7
9 0.763 0.160 14 23426834 missense variant G/A;C snv 0.700 1.000 14 1999 2019
dbSNP: rs121913630
rs121913630
MYH7
7 0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 0.710 1.000 13 1992 2018
dbSNP: rs121913638
rs121913638
MYH7
4 0.851 0.120 14 23425980 missense variant C/T snv 0.700 1.000 13 1994 2017
dbSNP: rs121913641
rs121913641
MYH7
3 0.882 0.080 14 23425970 missense variant C/G;T snv 0.700 1.000 13 1994 2013
dbSNP: rs727503278
rs727503278
MYH7
3 0.882 0.080 14 23432714 missense variant G/A;C;T snv 2.8E-05 0.700 1.000 11 2001 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 0.700 1.000 10 1999 2014
dbSNP: rs727503261
rs727503261
MYH7
3 0.882 0.080 14 23425774 missense variant A/G;T snv 0.700 1.000 10 2003 2015
dbSNP: rs397516088
rs397516088
MYH7
4 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 1.000 9 2003 2019
dbSNP: rs121913628
rs121913628
MYH7
10 0.763 0.160 14 23424059 missense variant C/G;T snv 0.700 1.000 8 1992 2017
dbSNP: rs193922390
rs193922390
MYH7 ; MHRT
3 0.882 0.080 14 23415651 missense variant C/G;T snv 4.0E-06; 2.0E-05 0.700 1.000 8 2008 2017
dbSNP: rs2754158
rs2754158
MYH7
4 0.882 0.080 14 23424876 missense variant G/A;C;T snv 1.2E-05 0.700 1.000 8 2004 2017
dbSNP: rs3218714
rs3218714
MYH7
9 0.763 0.160 14 23429279 missense variant G/A;C snv 0.700 1.000 8 1990 2013
dbSNP: rs397516260
rs397516260
MYH7
4 0.882 0.080 14 23431789 missense variant C/A;T snv 1.6E-05 0.700 1.000 8 2003 2017
dbSNP: rs45544633
rs45544633
MYH7 ; MHRT
4 1.000 0.080 14 23417174 missense variant G/A snv 0.700 1.000 8 2004 2013
dbSNP: rs727503260
rs727503260
MYH7
4 0.851 0.080 14 23425403 missense variant C/G;T snv 0.700 1.000 8 2003 2017
dbSNP: rs121913647
rs121913647
MYH7 ; MHRT
4 0.925 0.160 14 23417173 missense variant C/A;G;T snv 1.6E-05 0.700 1.000 7 2004 2013
dbSNP: rs397516157
rs397516157
MYH7
3 0.882 0.080 14 23424893 missense variant A/C;G;T snv 4.0E-06 0.700 1.000 7 2003 2017
dbSNP: rs397516178
rs397516178
MYH7
1 1.000 0.080 14 23422291 missense variant C/A;G;T snv 1.6E-05; 3.6E-05 0.700 1.000 7 2008 2017
dbSNP: rs397516248
rs397516248
MYH7 ; MHRT
6 0.851 0.200 14 23415153 missense variant C/T snv 0.700 1.000 7 2009 2017