Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 7
rs1875263
UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A8 ; UGT1A4
1.000 2 233716976 intron variant C/G;T snv 7
rs10173355
UGT1A9 ; UGT1A7 ; UGT1A10 ; UGT1A8
1.000 2 233688675 intron variant A/G;T snv 6
rs13241427 1.000 7 1249003 regulatory region variant G/T snv 0.72 6
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs2741012 1.000 2 233600317 upstream gene variant C/T snv 0.24 6
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 6
rs4663969
UGT1A6 ; UGT1A9 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A4 ; UGT1A8 ; UGT1A7
1.000 2 233746667 intron variant C/A;T snv 6
rs10039039
KCNIP1
1.000 5 170487960 intron variant C/T snv 8.9E-02 5
rs1005585
CBS
1.000 21 43056923 intron variant T/C snv 6.5E-02 5
rs10182825
PPP1CB ; SPDYA
1.000 2 28788221 intron variant G/A snv 9.0E-02 5
rs10467472
RGCC
1.000 13 41459562 intron variant G/C;T snv 5
rs10495970 1.000 2 49264671 intron variant G/A snv 0.26 5
rs10509586
LINC01374
1.000 10 89981680 intron variant G/T snv 7.1E-02 5
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
rs113974007 1.000 1 244750932 intergenic variant T/C snv 7.3E-02 5
rs11905359
TMEM230
1.000 20 5079306 intron variant C/A snv 7.1E-02 5
rs11933652 1.000 4 28961215 intergenic variant T/C snv 0.12 5
rs12532102
CDCA7L
1.000 7 21927090 intron variant A/G snv 0.82 5
rs12722486
IL2RA
1.000 10 6061799 intron variant C/A;T snv 5
rs1330950
LINC00551
1.000 13 106686453 intron variant C/A snv 0.62 5
rs13391004 1.000 2 136609937 intergenic variant G/A snv 9.1E-02 5
rs1349596
CADPS
1.000 3 62542448 intron variant C/T snv 6.3E-02 5
rs148332376
RHOH
1.000 4 40240870 intron variant -/T delins 7.0E-02 5
rs150933152
CLEC18B
1.000 16 74411734 missense variant C/T snv 5