Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10254101
PRKAG2
7 151718450 intron variant C/T snv 0.23 3
rs10265221
PRKAG2
7 151717243 intron variant T/A;C snv 3
rs10270542
PHTF2
7 77894452 intron variant A/G snv 0.43 2
rs10272546
KCTD7
7 66646470 intron variant A/G snv 0.51 1
rs10277115 7 1245559 regulatory region variant A/T snv 0.57 2
rs10283362 8 133320717 TF binding site variant C/T snv 0.24 1
rs1028455 14 88363631 regulatory region variant T/A snv 0.39 1
rs1031755
WDR72
15 53659238 intron variant A/C snv 0.22 1
rs1041331 13 60706983 intron variant A/T snv 0.35 1
rs1041606
MACROD2
20 14697142 intron variant C/T snv 0.21 1
rs10430743
EEF1AKMT2
10 124768428 intron variant T/G snv 0.55 1
rs10432479
NEB ; RIF1
2 151509261 intron variant T/C snv 0.61 1
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 3
rs1045463
TMEM60
7 77793835 3 prime UTR variant C/T snv 0.21 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10491128
FBXL20
17 39395735 intron variant G/A snv 0.32 1
rs10491967
TSPAN9
12 3258927 intron variant G/A snv 0.21 2
rs1050816
ASIC4-AS1 ; SPEG
2 219493476 3 prime UTR variant C/T snv 0.39 1
rs10513801
ETV5
3 186104564 intron variant T/G snv 9.2E-02 3
rs1051447
CWH43
4 49061855 missense variant C/A snv 0.65 0.58 1
rs10518732
WDR72
15 53646845 intron variant G/A;C snv 2
rs1055256
EEF1AKMT2
10 124758023 3 prime UTR variant A/G snv 0.54 1
rs10587862
TFDP2
3 142045613 intron variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTTTTTTT delins 1
rs10687766
RAI1
17 17688488 intron variant -/TAATAA delins 1
rs10715507
SLC9B2
4 103060542 intron variant TTTTTTT/-;T;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTTT delins 1