Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 1
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 2
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 1
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 3
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 1
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 1
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 1
rs2070635
AHSG
0.925 0.160 3 186618387 intron variant A/G snv 0.35 1
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 2
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 1
rs3792267
CAPN10
0.882 0.200 2 240591757 non coding transcript exon variant G/A snv 0.23 1
rs2073658
USF1
0.882 0.200 1 161040972 intron variant C/T snv 0.21 1
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 1
rs1799999
PPP1R3A
0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17 1
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 3
rs2975760
CAPN10
1.000 0.080 2 240591746 non coding transcript exon variant T/C snv 0.12 2
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 1