Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2859998
UBXN2B
0.882 0.080 8 58411603 intron variant G/A snv 0.30 4
rs12425451 0.882 0.080 12 3055757 TF binding site variant C/T snv 0.54 3
rs16830359 1.000 0.080 1 43130713 intergenic variant G/A;T snv 3
rs10049436 1.000 0.080 3 165771478 intron variant C/T snv 8.1E-02 2
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs1154155 0.925 0.080 14 22533736 upstream gene variant G/A;T snv 2
rs1540087
FOLR1
1.000 0.080 11 72190447 5 prime UTR variant G/A snv 3.8E-02 2
rs1551570
ANGPTL6 ; PPAN ; PPAN-P2RY11 ; SNORD105
0.925 0.080 19 10107354 intron variant C/T snv 0.59 2
rs17212223 0.925 0.080 6 32683763 intergenic variant C/T snv 0.19 2
rs2305795
EIF3G ; PPAN-P2RY11 ; P2RY11
0.925 0.080 19 10115376 intron variant G/A;C snv 2
rs3181077
CCR1 ; CCR3
1.000 0.080 3 46209161 intron variant C/T snv 0.80 2
rs3826784
EIF3G
0.925 0.080 19 10116334 non coding transcript exon variant A/G snv 0.58 2
rs5770917
CPT1B ; CHKB-CPT1B ; CHKB
0.925 0.080 22 50578924 intron variant T/C snv 6.0E-02 2
rs6907322
TSBP1-AS1 ; TSBP1
1.000 0.080 6 32357168 intron variant G/A snv 0.25 2
rs9268302
TSBP1-AS1 ; TSBP1
1.000 0.080 6 32357040 intron variant C/T snv 0.29 2
rs9274477
HLA-DQB1
0.925 0.080 6 32665936 intron variant A/G snv 2
rs10013443
PALLD
1.000 0.080 4 168685769 intron variant T/C snv 3.4E-02 1
rs10024442
TMEM131L
1.000 0.080 4 153570903 intron variant T/G snv 0.13 1
rs10032741 1.000 0.080 4 44958427 intergenic variant T/A;C snv 1
rs10035360 1.000 0.080 5 34604531 regulatory region variant C/T snv 0.19 1
rs10045595
TENM2
1.000 0.080 5 167802999 intron variant T/G snv 0.36 1
rs10091183 1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02 1
rs10094069
CSMD3
1.000 0.080 8 113022302 intron variant C/T snv 0.59 1
rs1009449
LOC105376617
1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03 1