Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs144851946
LMNA
1 156138701 missense variant G/A;T snv 1.4E-04; 4.0E-06 1
rs373584456
LMNA
1 156136335 missense variant C/T snv 2.4E-05 2.1E-05 1
rs374726751
LMNA
1 156136245 missense variant C/T snv 2.4E-05 3.5E-05 1
rs374926367
LMNA
1 156139089 missense variant A/G snv 1.2E-04 1.0E-04 1
rs59190448
OXTR ; CAV3
3 8761315 intron variant G/A snv 0.12 1
rs2020933
SLC6A4
17 30234737 intron variant A/T snv 0.14 1
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs1106076 1.000 0.080 7 5581212 regulatory region variant C/A;G snv 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs4680612 1.000 0.040 3 165891643 intergenic variant G/A snv 0.95 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs6024905
BPI
20 38329435 intron variant G/A snv 0.47 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2