Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1431648262
ADRA1A
8 26756585 3 prime UTR variant G/C snv 1.2E-05 2
rs771065515
LMNA
1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 2
rs1917760
LOC105375545 ; GSTK1 ; LOC105375546
7 143262206 intron variant G/A;T snv 1.8E-02 1
rs5767700
PPARA
22 46216775 intron variant T/C;G snv 1
rs5767743
PPARA
22 46226097 intron variant T/C snv 0.36 1
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs3862434
CRTC3
1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs1799904
LOC101929710 ; PCSK1
1.000 0.080 5 96429259 missense variant C/A;T snv 4.0E-06; 2.1E-03 2
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs150924946
LMNA
0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs267606841
GALNT3
0.882 0.120 2 165749801 missense variant A/C snv 5
rs7076156
ZNF365 ; LOC105378327
0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 3
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 7
rs763751076
AGXT
0.925 0.160 2 240875132 missense variant C/T snv 1.2E-05 6.3E-05 3
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs60662302
LMNA
0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9