Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
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
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
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
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 6
rs3124591
NOTCH1
0.827 0.120 9 136495945 3 prime UTR variant C/T snv 0.62 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
rs104893823
TNNC1
0.882 0.040 3 52451285 missense variant C/T snv 5