Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10199914 2 238975165 regulatory region variant A/G snv 0.39 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10281741
PTPRN2
7 158000430 intron variant G/A;C;T snv 1
rs10305923
EDNRA
4 147539622 intron variant T/C snv 2.1E-02 1
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs1037814
AFF1
4 87128698 intron variant T/C snv 0.60 3
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs10417097
PBX4
19 19609015 intron variant C/G snv 0.45 1
rs10419349
VAV1
19 6836678 intron variant C/T snv 2.5E-02 1
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs10438303 15 43724219 downstream gene variant T/C snv 0.16 1
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs10459452
ESR2
14 64245143 intron variant A/G snv 4.4E-03 1
rs10466588 11 116739533 regulatory region variant A/G snv 0.17 1
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10468274
NRN1L
16 67888439 intron variant G/A snv 0.31 2
rs10474433 5 75321018 intron variant T/C snv 0.36 1
rs10475588 5 173227744 upstream gene variant T/C snv 2.1E-02 1
rs10495712 2 20973240 intergenic variant A/G snv 0.77 1
rs1049817
GTF3C2
0.925 0.120 2 27328100 synonymous variant A/G snv 0.42 0.48 3