Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003688
SCGN
6 25658944 intron variant G/A snv 0.14 2
rs10049413
TRAIP
3 49855463 intron variant A/G snv 0.24 1
rs1007934
ZFYVE1
14 72996771 intron variant G/A snv 0.33 3
rs1008084
CCDC162P
6 109305762 intron variant G/A snv 0.40 3
rs1009110
COG1
17 73199810 intron variant C/T snv 0.52 1
rs10092747
TAF2
8 119736926 intron variant C/G;T snv 1
rs1010222
CALR
19 12937794 upstream gene variant A/G snv 0.70 3
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54 3
rs1011167
SP4
7 21489977 intron variant A/C snv 0.33 1
rs10137527 14 105134327 intron variant C/T snv 8.3E-02 1
rs10159477
HK1
10 69340132 intron variant G/A snv 0.14 3
rs10160596
EHBP1L1
11 65583893 non coding transcript exon variant G/A snv 0.20 3
rs10164806
ZEB2
2 144435759 intron variant C/T snv 6.7E-02 2
rs10165255
CYS1
2 10059474 intron variant A/G snv 0.59 2
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 4
rs10184620
PRKCE
2 46131396 intron variant A/G snv 0.12 2
rs10191559
UBE2E3
2 181075915 intron variant G/A snv 0.76 1
rs10197140
ACOXL
2 110852366 intron variant T/C snv 0.28 3
rs10205410
SPTBN1
2 54572462 intron variant G/T snv 0.31 1
rs1021797
ITPR2
12 26413499 intron variant A/C snv 4.7E-02 1
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs1022506
MYB
6 135190449 intron variant G/A snv 0.10 2
rs10226458 7 47595969 intergenic variant T/A snv 0.65 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10305916
EDNRA
4 147536174 intron variant T/G snv 0.21 1