Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3
rs2328549
CDKAL1
6 20718009 intron variant A/T snv 0.18 1
rs4746822
LOC101928994 ; HKDC1
10 69223185 non coding transcript exon variant C/T snv 0.59 1
rs587780343
GCK
7 44145638 missense variant C/A;T snv 1
rs587780347
GCK ; LOC105375258
7 44147807 missense variant C/T snv 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4