Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10082248
HSD11B1 ; HSD11B1-AS1
1.000 0.080 1 209693771 intron variant A/G;T snv 1
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs1021001 1.000 0.080 5 180777104 intergenic variant G/C;T snv 1
rs10246939
TAS2R38 ; MGAM
0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 6
rs1026520
MBP
1.000 0.080 18 77089350 intron variant C/A snv 0.73 1
rs1040070
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74512186 intron variant G/A;C snv 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10418248
UBL5
1.000 0.080 19 9827538 intron variant T/A;C snv 1
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042571
POMC
0.882 0.120 2 25161018 3 prime UTR variant G/A snv 0.16 3
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs10456444
CPNE5
1.000 0.080 6 36755065 non coding transcript exon variant T/C snv 0.44 1
rs10475
ATF3
1.000 0.080 1 212620271 3 prime UTR variant T/C snv 0.76 1
rs1048466
CCDC77
1.000 0.080 12 442384 3 prime UTR variant G/A;C snv 1
rs104894009
LOC105375258 ; GCK
0.882 0.120 7 44146587 missense variant C/G snv 3