Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11914494
IGSF11
3 119121264 intron variant G/A snv 1.8E-02 2
rs11926663
IGSF11
3 119125638 intron variant A/G snv 1.8E-02 2
rs141827060
IGSF11
3 119132020 intron variant C/T snv 1.8E-02 2
rs1461494 11 123055777 downstream gene variant T/A;C snv 2
rs16893073
C5orf17
5 24072508 intron variant C/G;T snv 2
rs17062789
DLGAP2
8 1203198 intron variant G/A;C snv 2
rs17062791
DLGAP2
8 1203431 intron variant C/T snv 0.14 2
rs1836778 4 29332870 intergenic variant T/C snv 0.56 2
rs1966678 4 29322410 intergenic variant T/G snv 0.60 2
rs2226150 6 77349634 intergenic variant G/A snv 0.49 2
rs2885296
UGT1A8 ; UGT1A9 ; UGT1A10 ; UGT1A5 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A4
2 233750415 intron variant A/C snv 0.30 2
rs2897639
LOC107985172
18 77568791 intergenic variant C/T snv 2.3E-02 2
rs34003842
DLGAP2
8 1206131 intron variant G/A;C;T snv 2
rs34213790
HLA-B
6 31350802 intron variant G/A snv 0.29 2
rs34352510
UGT1A9 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A5 ; UGT1A8 ; UGT1A4
2 233741916 non coding transcript exon variant T/C snv 0.33 2
rs4435343 18 43322011 intergenic variant C/A;T snv 2
rs4802
SNORD14E ; HSPA8
11 123057914 synonymous variant A/C;G snv 4.1E-06; 0.32 2
rs4936767 11 123047451 upstream gene variant A/G snv 0.34 2
rs4936770
HSPA8 ; SNORD14E
11 123058167 intron variant C/A;T snv 2
rs55920741 4 29331415 intergenic variant C/T snv 0.39 2
rs55980452
EBF2
8 26046363 upstream gene variant G/A snv 0.13 2
rs57580384 8 26048063 upstream gene variant G/A snv 0.14 2
rs59926619 8 26050704 intergenic variant G/A snv 0.13 2
rs638436 11 56495636 upstream gene variant G/A snv 0.58 2
rs638452 11 56495642 upstream gene variant A/T snv 0.58 2