Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10270542
PHTF2
7 77894452 intron variant A/G snv 0.43 2
rs1035940
INSR
19 7199967 intron variant C/A;G snv 1
rs1044299
PAPPA2
1 176842737 3 prime UTR variant C/G;T snv 2
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 2
rs10458575 1 65104082 regulatory region variant T/C snv 0.45 1
rs10460716
KCNJ6 ; DSCR4
21 38084132 intron variant T/A snv 0.53 1
rs10462028
TMEM165 ; CLOCK
0.882 0.120 4 55432133 3 prime UTR variant G/A snv 0.28 1
rs10464079 5 179098778 intergenic variant G/A snv 0.71 1
rs10475249 5 4010021 downstream gene variant C/G snv 0.45 1
rs10477191
FGF1
5 142698150 upstream gene variant A/G snv 0.22 1
rs10490869 3 35593653 intergenic variant A/T snv 0.15 1
rs10499013
LOC101927314
6 97498520 intron variant G/A;T snv 1
rs10501039 11 26152856 intergenic variant T/C snv 4.5E-02 1
rs10502148
ALG9
11 111777274 intron variant C/T snv 0.33 1
rs10507223 12 108062051 intergenic variant C/G snv 0.17 1
rs10507524
LINC00390 ; SMIM2-AS1
13 44110464 non coding transcript exon variant T/C snv 7.7E-02 1
rs10512606
RNF157
17 76215127 intron variant A/C snv 0.14 1
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 2
rs1053593
HMGXB4
22 35264882 missense variant G/C;T snv 8.0E-06; 0.58 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs10743098
SCUBE2 ; LOC105376541
11 9038003 intron variant A/G snv 0.42 1
rs10745659
CRADD
12 93698914 intron variant C/A;G snv 1
rs10752944
DNM3 ; LOC102724528 ; PIGC
1 172394384 non coding transcript exon variant C/T snv 0.47 1
rs10761785
REEP3
10 63559006 intron variant G/T snv 0.51 3