Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10199672
USP34
2 61400499 intron variant T/C;G snv 0.51 1
rs10202701
NCL
2 231463970 5 prime UTR variant C/A;T snv 1
rs10202845
COX7A2L
2 42348680 intron variant A/G snv 0.12 1
rs10203731 2 25678644 upstream gene variant C/G;T snv 1
rs10208141 2 6258395 non coding transcript exon variant T/C snv 0.66 1
rs10211501
LOC105373402
2 6399573 intergenic variant C/G snv 0.71 1
rs10218741
LOC101929750
1 221106893 regulatory region variant G/A;C snv 1
rs10221933
DIRC3-AS1
2 217281385 intron variant G/A;C snv 1
rs10228350
FOXP2
1.000 0.040 7 114420608 intron variant A/G;T snv 2
rs10231759 7 150815084 regulatory region variant T/C snv 0.41 2
rs10232036
BBS9
7 33212340 intron variant T/C snv 0.17 1
rs10236314
ABCB5
7 20676586 intron variant A/C snv 0.90 1
rs10250729
ZNRF2P1 ; DPY19L1P1
7 32745115 intron variant T/C snv 0.16 1
rs10253161 7 46956794 intron variant A/G snv 0.32 1
rs10253861
GLCCI1
7 8070845 non coding transcript exon variant G/A snv 0.56 1
rs10271999 7 27469589 intergenic variant G/A snv 0.44 1
rs10276670
AQP1
7 30916874 intron variant A/G snv 0.29 1
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs1029534
JAZF1
7 28149464 intron variant T/C;G snv 2
rs10305677
ARNT
1 150846616 intron variant T/A snv 1.8E-02 1
rs1036034
KLHL5
4 39105299 intron variant A/G snv 0.47 1
rs1036821
ZFAT
8 134638240 intron variant G/A snv 0.28 2
rs1038694
BABAM2 ; LOC100505736
2 28150685 intron variant A/G snv 0.73 1
rs1039440 5 51204794 intergenic variant A/G snv 0.48 1
rs10401193
GATAD2A
19 19480257 intron variant A/G snv 0.19 2