Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 1
rs2070634
AHSG
1.000 0.080 3 186618238 intron variant T/G snv 0.47 1
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 1
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 1
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 1
rs4512367
PREX2
1.000 0.080 8 68015357 intron variant C/T snv 0.44 1
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 1
rs203462
AKAP10
0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 1
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 3
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 2
rs182549
MCM6
2 135859184 intron variant C/T snv 0.41 1
rs279845
GABRA2
1.000 0.080 4 46327706 intron variant T/A snv 0.41 1
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 1
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 1
rs745379
GATA4
8 11758186 intron variant A/G snv 0.39 1
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 3
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 1
rs9660525
MIR181A1HG
1.000 0.040 1 198807802 non coding transcript exon variant C/A snv 0.38 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 1
rs279836
GABRA2
4 46337053 intron variant T/A snv 0.38 1
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 1
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 1
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 1
rs642742 12 88905969 intergenic variant C/T snv 0.37 1