Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10980457
SVEP1
9 110576455 intron variant A/C snv 9.8E-02 1
rs12572168
ADD3-AS1 ; ADD3
10 110005028 intron variant A/C snv 0.14 1
rs139939228 5 132528343 intron variant A/C snv 5.1E-03 1
rs184853555 11 49933299 intergenic variant A/C snv 3.5E-03 1
rs2847273
PTPN2
18 12856909 intron variant A/C snv 0.34 1
rs34224666
RAP1GAP2 ; LOC101927911
17 2962495 non coding transcript exon variant A/C snv 0.24 1
rs4912892
ARHGAP26
5 143046673 intron variant A/C snv 0.49 1
rs55756407 7 20593249 downstream gene variant A/C snv 1.3E-02 1
rs7150940 14 60223913 intergenic variant A/C snv 0.38 1
rs75526024
CCR1 ; CCR3
3 46208969 intron variant A/C snv 4.0E-02 1
rs7649379
GCSAM ; C3orf52
3 112121666 3 prime UTR variant A/C snv 4.9E-02 1
rs9349322 6 45666355 downstream gene variant A/C snv 0.28 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 6
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs7192652
NLRC5
16 57041268 intron variant A/C;G snv 2
rs8017228
STXBP6
14 24980020 intron variant A/C;G snv 2
rs10241173 7 124813204 intergenic variant A/C;G snv 1
rs111526888 18 60304392 downstream gene variant A/C;G snv 1
rs117407105 2 136168220 regulatory region variant A/C;G snv 1
rs3016175
LOC105369325
11 61062895 intron variant A/C;G snv 1
rs34108746
PRG3
11 57378752 missense variant A/C;G snv 4.0E-06; 5.9E-02 1
rs395892
CLC
19 39735635 intron variant A/C;G snv 1
rs4887991
WWOX
16 78887166 intron variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99