Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2294882
TSBP1-AS1 ; BTNL2
6 32399738 intron variant T/C snv 0.19 2
rs1062630
POU5F1
6 31170330 synonymous variant G/A snv 0.18 0.22 1
rs10885
PRRC2A
6 31636814 missense variant C/T snv 0.14 0.17 1
rs1161098
LOC105369812 ; LINC02408
12 67453680 intron variant G/A snv 0.84 1
rs116671518
DKK2
4 107189709 intron variant T/C snv 1.9E-02 1
rs12154141 6 62460168 downstream gene variant A/C snv 0.20 1
rs138117677 16 3348899 TF binding site variant GGGACT/- delins 2.8E-02 1
rs200655768
TTN-AS1 ; TTN
2 178711222 synonymous variant G/A;T snv 1
rs200688486 6 32621223 regulatory region variant -/T delins 1
rs204992
PBX2
6 32189131 intron variant G/A snv 0.22 1
rs2153486 14 87737048 intron variant C/T snv 0.68 1
rs2294884
TSBP1-AS1 ; BTNL2
6 32399482 intron variant T/A;G snv 0.18 1
rs28362680
BTNL2 ; TSBP1-AS1
6 32403039 missense variant G/A snv 0.14 0.12 1
rs3104369
HLA-DQA1
6 32634705 intron variant T/C snv 0.71 1
rs3130070
PRRC2A
6 31624031 intron variant A/G snv 0.17 1
rs3130623
PRRC2A
6 31629923 intron variant C/T snv 0.18 1
rs314879 13 22735243 intergenic variant C/T snv 0.78 1
rs5861895 4 129344228 regulatory region variant TT/-;T;TTT delins 1
rs594418
NRG3
10 82625296 intron variant G/A snv 0.83 1
rs6105452
MACROD2
20 15683126 intron variant C/T snv 0.10 1
rs62309385 4 136134743 intron variant G/C snv 9.8E-02 1
rs6797827 3 109735523 intron variant C/T snv 0.18 1
rs80274284
SLC22A15
1 116037356 missense variant G/T snv 1
rs9267536
LOC105375019 ; LY6G5C
6 31683417 intron variant A/C snv 5.3E-02 1
rs9271488 6 32621223 regulatory region variant G/T snv 0.27 1