Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4236746 8 129687615 non coding transcript exon variant A/G snv 0.99 1
rs1516527
CPA3
3 148891917 intron variant T/C snv 0.97 1
rs1859161 4 105121535 downstream gene variant C/T snv 0.95 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7537229 1 56440602 intron variant G/A snv 0.92 4
rs177251
PCBD2 ; CATSPER3
5 135007779 intron variant G/A snv 0.92 1
rs1013910 1 116868761 intergenic variant G/A snv 0.91 1
rs1994712
SLC35A5
3 112585396 3 prime UTR variant T/C snv 0.91 1
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs10195713 2 157664393 intergenic variant C/T snv 0.89 1
rs360124
LOC105369149 ; SBF2 ; SBF2-AS1
11 9780681 non coding transcript exon variant G/C snv 0.88 1
rs762679
MCM4
8 47972876 missense variant T/A snv 0.87 0.88 4
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs2514594
SAMD12
8 118612910 intron variant G/A snv 0.86 1
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs2695478
MPHOSPH9
12 123204974 intron variant C/T snv 0.84 1
rs7781571 7 106787724 intron variant A/G snv 0.84 1
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs990211
NCKIPSD
3 48683607 intron variant A/G snv 0.83 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs2114718 15 70640951 downstream gene variant G/A snv 0.82 1
rs1586068
IKZF2
2 213033508 intron variant A/G snv 0.81 2
rs301161
EMC8
16 85776743 intron variant G/A snv 0.81 2