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: 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
dbSNP: rs369437262
rs369437262
MYH7 ; MHRT
1 1.000 0.080 14 23415228 missense variant T/C snv 3.2E-05 6.3E-05 0.700 1.000 27 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: rs145677314
rs145677314
MYH7
1 1.000 0.080 14 23425346 missense variant G/A snv 5.6E-05 8.4E-05 0.700 1.000 23 1992 2014
dbSNP: rs372381770
rs372381770
MYH7 ; MHRT
2 0.925 0.080 14 23414101 missense variant G/A snv 2.4E-05 2.1E-05 0.700 1.000 23 1992 2014
dbSNP: rs397516098
rs397516098
MYH7
3 0.882 0.080 14 23429044 missense variant C/T snv 0.700 1.000 23 1992 2014
dbSNP: rs397516201
rs397516201
MYH7 ; MIR208B
3 0.882 0.080 14 23418249 missense variant G/A snv 4.0E-06 1.4E-05 0.700 1.000 23 1992 2014
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: 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: 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: rs200939753
rs200939753
MYH7 ; MHRT
1 1.000 0.080 14 23415225 missense variant C/T snv 6.8E-05 9.1E-05 0.700 1.000 20 1992 2005
dbSNP: rs201307101
rs201307101
MYH7 ; MHRT
2 0.925 0.080 14 23417295 missense variant C/A;G;T snv 3.0E-04; 4.0E-06 0.700 1.000 20 1992 2005
dbSNP: rs201895208
rs201895208
MYH7 ; MIR208B ; MHRT
1 1.000 0.080 14 23417616 missense variant G/T snv 0.700 1.000 20 1992 2005
dbSNP: rs2069544
rs2069544
MYH7
3 0.882 0.080 14 23425371 missense variant G/A;C;T snv 2.9E-04 0.700 1.000 20 1992 2005
dbSNP: rs3218715
rs3218715
MYH7
1 1.000 0.080 14 23428583 missense variant C/T snv 0.700 1.000 20 1992 2005
dbSNP: rs397516088
rs397516088
MYH7
4 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 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: rs397516097
rs397516097
MYH7
2 0.925 0.080 14 23429089 missense variant C/T snv 0.700 1.000 20 1992 2005
dbSNP: rs397516139
rs397516139
MYH7
2 0.925 0.080 14 23425752 missense variant C/G;T snv 0.700 1.000 20 1992 2005
dbSNP: rs397516160
rs397516160
MYH7
2 0.925 0.080 14 23424804 stop gained G/A;C snv 0.700 1.000 20 1992 2005
dbSNP: rs397516170
rs397516170
MYH7
1 1.000 0.080 14 23424050 stop gained C/A;T snv 0.700 1.000 20 1992 2005
dbSNP: rs397516179
rs397516179
MYH7
1 1.000 0.080 14 23422256 missense variant C/T snv 8.0E-06 7.0E-06 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: rs397516222
rs397516222
MYH7 ; MHRT
1 1.000 0.080 14 23416975 missense variant T/A snv 0.700 1.000 20 1992 2005
dbSNP: rs397516241
rs397516241
MYH7 ; MHRT
1 1.000 0.080 14 23415252 missense variant C/T snv 0.700 1.000 20 1992 2005