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: rs104894369
rs104894369
MYL2
10 0.807 0.080 12 110914287 missense variant C/A;T snv 0.030 1.000 3 2019 2019
dbSNP: rs35049558
rs35049558
MYL2
8 0.851 0.040 12 110914287 frameshift variant -/CT ins 8.0E-06 0.030 1.000 3 2019 2019
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: rs199476301
rs199476301
TPM1
6 0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs199476320
rs199476320
TPM1
3 0.925 0.040 15 63064121 missense variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs199476321
rs199476321
TPM1
3 0.882 0.080 15 63064133 missense variant T/C snv 4.0E-06 1.4E-05 0.010 1.000 1 2019 2019
dbSNP: rs199476322
rs199476322
TPM1
2 0.925 0.040 15 63064141 missense variant A/G snv 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs730880751
rs730880751
MYH7
2 0.925 0.040 14 23424816 missense variant C/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs915012109
rs915012109
SMYD1
3 0.925 0.040 2 88096710 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1060501436
rs1060501436
MYH7
2 0.925 0.040 14 23424815 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs1157637439
rs1157637439
VARS2
4 0.882 0.120 6 30920187 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs1199713333
rs1199713333
CACNA1C
2 0.925 0.040 12 2593318 missense variant C/T snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1412710023
rs1412710023
MYBPC3
3 0.925 0.040 11 47343549 missense variant T/A snv 4.1E-06 0.010 1.000 1 2018 2018
dbSNP: rs371401403
rs371401403
MYBPC3
6 0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 0.010 1.000 1 2018 2018
dbSNP: rs397516406
rs397516406
MYL2
2 0.925 0.040 12 110911093 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs751224055
rs751224055
CACNA1C
2 0.925 0.040 12 2674574 missense variant C/A;T snv 5.2E-06; 5.2E-06 0.010 1.000 1 2018 2018
dbSNP: rs104894231
rs104894231
HRAS ; LRRC56
9 0.776 0.360 11 533467 missense variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs397516130
rs397516130
MYH7
3 0.882 0.080 14 23426033 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs398123226
rs398123226
GLA ; RPL36A-HNRNPH2
3 0.882 0.160 X 101398403 missense variant G/C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs60890628
rs60890628
LMNA
9 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 0.010 1.000 1 2017 2017
dbSNP: rs730880460
rs730880460
HRAS ; LRRC56
3 0.882 0.120 11 533877 missense variant C/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs754945616
rs754945616
RASA1
3 0.882 0.120 5 87268639 missense variant G/T snv 4.2E-06 0.010 1.000 1 2017 2017
dbSNP: rs104894833
rs104894833
GLA ; RPL36A-HNRNPH2
11 0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 0.010 1.000 1 2016 2016
dbSNP: rs1057517686
rs1057517686
ATAD3A
7 0.827 0.120 1 1529299 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs121917758
rs121917758
HRAS ; LRRC56
4 0.851 0.160 11 533883 missense variant G/A snv 0.010 1.000 1 2016 2016