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: rs730880759
rs730880759
MYH7
2 0.925 0.080 14 23424068 stop gained C/A;T snv 4.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs1057517773
rs1057517773
MYH7
1 1.000 0.080 14 23431641 missense variant C/T snv 0.700 1.000 3 2016 2017
dbSNP: rs727504311
rs727504311
MYH7
3 0.882 0.080 14 23424905 missense variant T/C snv 0.700 1.000 4 2015 2018
dbSNP: rs730880883
rs730880883
MYH7
1 1.000 0.080 14 23426809 missense variant C/T snv 0.700 1.000 2 2014 2017
dbSNP: rs730880781
rs730880781
MYH7 ; MIR208B
1 1.000 0.080 14 23419949 missense variant C/G;T snv 4.0E-06 0.700 1.000 2 2013 2014
dbSNP: rs869025477
rs869025477
MYH7
1 1.000 0.080 14 23429308 missense variant G/A snv 0.700 1.000 1 2013 2013
dbSNP: rs727504239
rs727504239
MYH7
3 0.882 0.080 14 23427242 missense variant T/C snv 4.0E-06 7.0E-06 0.700 1.000 9 2011 2017
dbSNP: rs397516165
rs397516165
MYH7
4 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 1.000 5 2011 2017
dbSNP: rs727504385
rs727504385
MYH7 ; MHRT
1 1.000 0.080 14 23415210 missense variant T/C snv 0.700 1.000 5 2011 2017
dbSNP: rs1060501448
rs1060501448
MYH7
1 1.000 0.080 14 23425792 missense variant A/G snv 0.700 1.000 4 2011 2017
dbSNP: rs2856897
rs2856897
MYH7
2 0.925 0.080 14 23424875 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 0.700 1.000 4 2011 2017
dbSNP: rs730880800
rs730880800
MYH7 ; MIR208B ; MHRT
1 1.000 0.080 14 23417556 missense variant G/A snv 0.700 1.000 4 2011 2017
dbSNP: rs1060501443
rs1060501443
MYH7
1 1.000 0.080 14 23427855 missense variant A/G snv 0.700 1.000 3 2011 2017
dbSNP: rs1224554825
rs1224554825
MYH7
1 1.000 0.080 14 23425991 missense variant C/A;T snv 1.4E-05 0.700 1.000 3 2011 2017
dbSNP: rs1566537070
rs1566537070
MYH7
1 1.000 0.080 14 23431473 missense variant G/T snv 0.700 1.000 3 2011 2017
dbSNP: rs1131691685
rs1131691685
MYH7
1 1.000 0.080 14 23427672 missense variant G/A;C snv 0.700 1.000 2 2011 2017
dbSNP: rs121913633
rs121913633
MYH7
3 0.882 0.080 14 23431447 missense variant C/T snv 7.0E-06 0.700 1.000 2 2011 2017
dbSNP: rs1555337794
rs1555337794
MYH7
1 1.000 0.080 14 23425294 missense variant A/G snv 0.700 1.000 2 2011 2017
dbSNP: rs397516220
rs397516220
MYH7 ; MHRT
2 0.925 0.160 14 23416988 splice acceptor variant CTC/- delins 0.700 1.000 2 2011 2015
dbSNP: rs727504236
rs727504236
MYH7
3 0.882 0.080 14 23428642 missense variant T/C snv 0.700 1.000 2 2011 2017
dbSNP: rs727504283
rs727504283
MYH7
2 0.925 0.080 14 23431804 missense variant G/A snv 0.700 1.000 2 2011 2017
dbSNP: rs730880159
rs730880159
MYH7
2 0.925 0.080 14 23429031 missense variant T/A;C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs397516248
rs397516248
MYH7 ; MHRT
6 0.851 0.200 14 23415153 missense variant C/T snv 0.700 1.000 7 2009 2017
dbSNP: rs397516264
rs397516264
MYH7
9 0.763 0.160 14 23431602 missense variant C/T snv 4.0E-06 0.700 1.000 7 2009 2017
dbSNP: rs727504310
rs727504310
MYH7
3 0.882 0.080 14 23424909 missense variant T/C snv 0.700 1.000 6 2009 2017