Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10929178
USP40
2 233487920 3 prime UTR variant G/C;T snv 2
rs11675858
USP40
2 233531407 intron variant G/A;C snv 2
rs11676524
USP40
2 233552322 intron variant A/T snv 0.13 2
rs11683101
USP40
2 233490079 intron variant T/C snv 2.3E-02 2
rs11686188
USP40
2 233542984 intron variant G/A snv 0.12 2
rs12472244
USP40
2 233558197 intron variant A/G snv 0.19 2
rs13385018
USP40
2 233547610 intron variant C/T snv 2.1E-02 2
rs3796090
USP40
2 233481956 intron variant T/C snv 0.19 2
rs3796092
USP40
2 233481823 intron variant C/A snv 0.13 2
rs4047189
USP40
2 233534303 intron variant G/T snv 0.13 2
rs4047198
USP40
2 233546254 non coding transcript exon variant C/A;G snv 2
rs6704644
USP40
2 233498009 intron variant G/T snv 9.2E-02 2
rs6746234
USP40
2 233524435 intron variant G/A snv 0.13 2
rs3755321
UGT1A9 ; UGT1A8 ; UGT1A7 ; UGT1A10 ; UGT1A6 ; UGT1A5
2 233713179 missense variant T/C snv 0.12 9.9E-02 2
rs6737107
UGT1A9 ; UGT1A8 ; UGT1A7 ; UGT1A10
2 233687549 intron variant G/A snv 1.6E-03 2
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 9
rs7572563
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
2 233708590 non coding transcript exon variant G/A snv 0.58 3
rs7563561
UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7 ; UGT1A6
2 233690345 intron variant T/C;G snv 3
rs4347832
UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
2 233684395 intron variant T/C snv 0.39 3
rs7586110
UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
2 233681881 intron variant T/A;G snv 3
rs7579530
UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
2 233679939 intron variant G/A snv 0.65 2
rs12615708
UGT1A9 ; UGT1A8 ; UGT1A10
2 233675200 intron variant G/A snv 8.2E-02 2
rs17864684
UGT1A9 ; UGT1A8 ; UGT1A10
2 233670717 intron variant G/A snv 0.15 2
rs17868322
UGT1A9 ; UGT1A8 ; UGT1A10
2 233671848 intron variant G/A snv 2.3E-02 2
rs2602379
UGT1A9 ; UGT1A8 ; UGT1A10
2 233674416 intron variant G/A snv 0.62 2