Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805124
SCN5A
0.742 0.280 3 38603929 missense variant T/C snv 0.22 0.25 16
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 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
rs3747517
IFIH1
0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
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
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 9
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs4758680
LRRC43
0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs150840924
LMNA
0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 7