Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59374417 0.925 0.040 3 119569567 intergenic variant A/C;T snv 2
rs10503019
ATP8B1
0.925 0.040 18 57787145 intron variant G/A snv 0.17 2
rs35677492
CAT
0.925 0.040 11 34471409 synonymous variant G/A snv 5.0E-04 2.7E-04 2
rs158676
CDK5RAP1
0.925 0.040 20 33386589 intron variant G/A snv 0.68 2
rs11940117
CLNK
0.925 0.040 4 10725083 intergenic variant C/G;T snv 2
rs613791
CXCR5
0.925 0.040 11 118893342 intron variant C/T snv 0.34 2
rs2267641
DDR1
0.925 0.040 6 30897427 synonymous variant A/C snv 0.24 0.18 2
rs4618569
DDR1
0.925 0.040 6 30887474 intron variant G/A snv 0.25 2
rs1298695421
HP ; TXNL4B
0.925 0.040 16 72060682 missense variant C/T snv 7.0E-06 2
rs71453838
LOC112268097 ; PFDN5 ; C12orf10
0.925 0.040 12 53299748 missense variant AA/GC mnv 2
rs1534284
PFDN5 ; LOC112268097 ; C12orf10
0.925 0.040 12 53299748 missense variant A/G;T snv 0.99; 4.0E-06 2
rs2071464
PSMB8
0.925 0.040 6 32841299 intron variant G/A snv 0.43 2
rs1417210
SLC29A3
0.925 0.040 10 71376162 intron variant G/A;C snv 2
rs11575993
SOD2
0.925 0.040 6 159688219 missense variant G/A snv 2
rs760870035
TAP1 ; PSMB9
0.925 0.040 6 32854240 missense variant C/G;T snv 1.4E-05; 1.4E-05 2
rs1408944
ZMIZ1
0.925 0.040 10 79248726 intron variant A/G snv 0.25 2
rs6960920 0.925 0.040 7 44376473 downstream gene variant G/C;T snv 0.37 3
rs734930
AUTS2
0.925 0.040 7 70555174 intron variant T/C snv 0.53 3
rs10431924
CDH1
0.882 0.120 16 68805399 intron variant T/C snv 0.45 3
rs291700
CDK5RAP1
0.925 0.040 20 33394043 synonymous variant T/C snv 0.64 0.62 3
rs523604
CXCR5
0.882 0.120 11 118885029 intron variant A/G snv 0.53 3
rs2039381
IFNE ; MIR31HG
0.882 0.040 9 21481484 stop gained G/A snv 4.5E-02 3.7E-02 3
rs12301088
IFNG-AS1
0.882 0.080 12 68196168 intron variant C/T snv 0.37 3
rs4744411
LOC101928119 ; AOPEP
0.925 0.040 9 94926763 intron variant G/A;C;T snv 3
rs2273844
LOC107984667 ; GZMB
0.925 0.040 14 24634208 5 prime UTR variant G/A snv 0.24 0.26 3