Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199865688
MYBPC3
0.925 0.080 11 47337496 missense variant C/T snv 1.5E-03 1.2E-03 4
rs387906816
GATA6
0.882 0.080 18 22171695 missense variant G/A snv 8.4E-04 1.5E-04 4
rs56208331
GATA4
0.925 0.080 8 11758419 missense variant G/A;T snv 2.0E-03 4
rs1393297693
SRF
1.000 0.040 6 43178806 missense variant G/A snv 4.0E-06 3
rs2228638
NRP1
1.000 0.080 10 33186354 missense variant C/T snv 0.12 9.4E-02 3
rs387906772
GATA4
1.000 0.080 8 11755064 missense variant A/G;T snv 3
rs746503158
MTG1
1.000 0.040 10 133420125 missense variant A/G;T snv 8.0E-06; 4.0E-06 3
rs764328696
TBX20
1.000 7 35248696 missense variant C/G;T snv 3
rs769402060
CYP1B1-AS1 ; CYP1B1
0.925 0.120 2 38075022 missense variant A/G snv 3.3E-05 4.2E-05 3
rs104893900
NKX2-5
1.000 5 173233011 missense variant G/A snv 2
rs137852952
TLL1
1.000 0.080 4 166003471 missense variant T/C snv 2.1E-04 2.4E-04 2
rs199715380
CFC1
2 130597533 missense variant C/T snv 2
rs387906771
GATA4
1.000 0.080 8 11750166 missense variant C/G;T snv 2
rs746365549
TTN
2 178782573 missense variant C/A;T snv 8.0E-06 2
rs758277832
NKX2-5
1.000 0.080 5 173233109 missense variant G/C snv 2
rs759067821
GATA4
1.000 0.080 8 11758294 missense variant C/T snv 2.8E-05 1.4E-05 2
rs111862418
TBX20
7 35204548 missense variant A/C;T snv 1
rs1346496644
CCN1
1 85581440 missense variant C/G;T snv 1
rs1390448535
NOS3
7 151007245 missense variant C/G snv 4.2E-06 1
rs147405081
TBX5
12 114366360 missense variant C/T snv 1.2E-03 4.1E-03 1
rs2579433
CFC1B
2 130522115 missense variant T/A;C snv 1
rs375349466
TLL1
4 166003545 missense variant A/G snv 8.0E-06 2.8E-05 1
rs483352999
TBX20
7 35202590 missense variant A/C snv 1
rs753669213
LBX2
2 74498109 missense variant T/C snv 1.7E-04 1.8E-04 1
rs768000961
CCNA2
4 121823490 missense variant G/A snv 8.1E-06 1