Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs144983009 5 56792072 intergenic variant C/T snv 5.7E-02 2
rs1658972 9 6665010 intron variant C/A;T snv 2
rs201022 6 6669940 intergenic variant C/A;T snv 2
rs2024641 22 35734507 downstream gene variant G/A snv 0.29 2
rs2383733 9 27869512 intergenic variant A/G;T snv 2
rs7122144 11 129520077 intergenic variant T/C snv 0.16 2
rs76861960 16 77565542 intergenic variant T/C snv 1.3E-02 2
rs7803882 7 55869748 intergenic variant T/A;C snv 2
rs8108722 19 10236408 intergenic variant T/A;C snv 2
rs8182496 19 31643033 intergenic variant C/T snv 0.46 2
rs9601485 13 80901307 intron variant C/T snv 0.28 2
rs4979372
AKNA
9 114377802 intron variant T/C;G snv 2
rs9436480
CDCP2
1 54151583 intron variant A/G snv 8.9E-02 2
rs754465
DLG5
10 77920756 intron variant C/A snv 0.52 2
rs10787429
GPAM
10 112189906 intron variant T/A;C snv 2
rs200088103
GPT ; LOC101928953
8 144505033 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.0E-04 2
rs13247499
JAZF1
7 28139639 intron variant C/A snv 0.10 2
rs185355701
LOC105375026 ; LINC01016
6 33893066 intron variant G/A;T snv 2
rs9940874
MARF1
16 15634417 intron variant T/C snv 0.18 2
rs17801127
MMADHC-DT
2 149707970 intron variant C/T snv 8.6E-02 2
rs73186036
N6AMT1
21 28754160 regulatory region variant A/G snv 0.20 2
rs45587331
PIK3AP1
10 96700824 non coding transcript exon variant G/A snv 0.13 2
rs111532669
PTCH1
9 95446682 3 prime UTR variant C/T snv 1.8E-02 2
rs11124554
STRN
2 36922355 intron variant T/A;C snv 2
rs62269283
TM4SF4
3 149494481 intron variant G/A snv 1.9E-02 2