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: rs121913624
rs121913624
MYH7
4 0.851 0.080 14 23429278 missense variant C/A;G;T snv 0.030 1.000 3 2014 2018
dbSNP: rs121913630
rs121913630
MYH7
7 0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 0.030 1.000 3 2006 2020
dbSNP: rs1060501436
rs1060501436
MYH7
2 0.925 0.040 14 23424815 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs1064793206
rs1064793206
MYH7
2 0.925 0.040 14 23424993 missense variant G/A snv 0.010 1.000 1 2010 2010
dbSNP: rs121913625
rs121913625
MYH7
4 0.851 0.080 14 23429005 missense variant G/A;C;T snv 0.010 1.000 1 2003 2003
dbSNP: rs121913627
rs121913627
MYH7
8 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs121913634
rs121913634
MYH7
3 0.882 0.080 14 23425372 missense variant T/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs121913652
rs121913652
MYH7 ; MHRT
3 0.882 0.080 14 23414015 missense variant C/T snv 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1489940065
rs1489940065
MYH7
2 0.925 0.040 14 23433188 missense variant G/A snv 2.8E-05 7.7E-05 0.010 1.000 1 2008 2008
dbSNP: rs36211715
rs36211715
MYH7
5 0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs397516130
rs397516130
MYH7
3 0.882 0.080 14 23426033 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs730880742
rs730880742
MYH7
3 0.882 0.080 14 23424984 missense variant T/A;C;G snv 0.010 1.000 1 2003 2003
dbSNP: rs730880751
rs730880751
MYH7
2 0.925 0.040 14 23424816 missense variant C/A;G snv 0.010 1.000 1 2019 2019