Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10011838 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 3
rs10039206 5 56692951 intergenic variant T/C snv 0.61 2
rs10049088
LINC02029
3 157079859 upstream gene variant C/T snv 0.35 3
rs10065892
AP3B1
5 78267439 intron variant G/A snv 0.27 2
rs10071838
MIR580 ; LMBRD2
5 36147704 intron variant C/A;T snv 2
rs10099100 8 10719265 downstream gene variant G/C snv 0.32 3
rs10132033
PPP1R36
14 64556852 intron variant T/C snv 0.16 2
rs10132060
SLC7A8
14 23128526 intron variant C/T snv 0.13 2
rs10159676 10 50302023 downstream gene variant G/A snv 0.34 2
rs10194817
WDCP ; MFSD2B ; FKBP1B
2 24034181 intron variant A/G;T snv 2
rs10210385
LINC01122
2 58770577 intron variant T/C snv 0.40 2
rs10223451 6 139630553 intron variant A/G snv 0.58 2
rs10224902
ANLN
7 36415868 synonymous variant T/C snv 0.13 0.12 2
rs10254125
EIF2AK1
7 6027315 intron variant A/G snv 0.65 2
rs10263707
PRKAG2
7 151706419 intron variant T/G snv 0.31 2
rs1029555 7 26547477 upstream gene variant T/C snv 0.80 2
rs10405535
PDCD5
19 32581179 upstream gene variant A/G;T snv 2
rs10410723
RAB8A
19 16124498 non coding transcript exon variant C/A snv 0.19 2
rs10410869 19 57629913 upstream gene variant G/T snv 0.12 2
rs10414846
HAMP
19 35281568 intron variant C/T snv 0.21 3
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10424080 19 18407968 TF binding site variant C/T snv 0.29 2
rs10424619
USF2
19 35277334 non coding transcript exon variant A/G;T snv 2
rs1043897
GALNT2
1 230280653 3 prime UTR variant G/T snv 0.49 2
rs10448
CENPBD1P1
19 58581872 non coding transcript exon variant T/C snv 0.53 2