Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3736594
MRPL33
2 27772914 intron variant A/C snv 0.62 3
rs4663967
UGT1A9 ; UGT1A5 ; UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; DNAJB3 ; UGT1A4 ; UGT1A6
2 233744538 intron variant A/C snv 0.55 3
rs6753320
UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
2 233686969 intron variant A/C snv 0.39 3
rs6753569
UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A10
2 233687171 intron variant A/C snv 0.39 3
rs9637599
PPM1K ; PPM1K-DT
4 88285078 intron variant A/C snv 0.56 3
rs12196873
MFSD4B
6 111276855 3 prime UTR variant A/C snv 0.10 2
rs61896141
MYRF ; TMEM258
11 61788567 intron variant A/C snv 0.11 2
rs6690733
DOCK7
1.000 0.080 1 62594640 intron variant A/C snv 0.43 2
rs7212936
SERPINF2
17 1743357 intron variant A/C snv 0.46 2
rs10141869
LOC105370504
14 53665936 intron variant A/C snv 0.20 1
rs1037920
ARNTL2-AS1 ; ARNTL2
12 27400808 intron variant A/C snv 0.19 0.13 1
rs1052335
TPD52L3
9 6330380 3 prime UTR variant A/C snv 0.17 1
rs1061388
REV3L ; MFSD4B
6 111299091 3 prime UTR variant A/C snv 0.10 1
rs10741271 10 127467534 intergenic variant A/C snv 0.79 1
rs10872069
TRAF3IP2-AS1
6 111540523 intron variant A/C snv 0.47 1
rs10883092
PYROXD2
10 98407519 intron variant A/C snv 0.37 1
rs10889340
DOCK7
1 62546400 intron variant A/C snv 0.58 1
rs10897203 11 62011041 downstream gene variant A/C snv 0.99 1
rs11050764
LINC02386
12 30260219 intron variant A/C snv 0.30 1
rs11153280
MFSD4B
6 111268090 3 prime UTR variant A/C snv 0.41 1
rs1148259
ANKRD30A
10 37219522 synonymous variant A/C snv 0.50 0.44 1
rs11601659
KCNJ1 ; LOC107984409
11 128858992 intron variant A/C snv 5.9E-02 1
rs11632157
MYO1E
15 59183889 intron variant A/C snv 0.83 1
rs11854656
LIPC ; ALDH1A2
15 58420746 intron variant A/C snv 0.26 1
rs11856833
AGBL1
15 86264653 synonymous variant A/C snv 0.18 0.17 1