Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs4758680
LRRC43
0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 9
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 6
rs267607124
TNNC1
0.807 0.080 3 52451410 missense variant G/A;C;T snv 4.0E-05; 4.0E-06; 1.3E-04 6
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 6