Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs2908289
GCK ; LOC105375257
1.000 0.080 7 44184343 intron variant G/A snv 0.20 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs11039119
MIR6745 ; PACSIN3
11 47180373 intron variant G/A snv 0.38 0.33 2
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs2390732
CERS6
2 168749457 intron variant G/A snv 0.65 2
rs3778321
RREB1
6 7250037 3 prime UTR variant G/A snv 0.11 2
rs3829109
CARD9 ; DNLZ
9 136362314 intron variant G/A snv 0.25 2
rs5394
SLC2A2
3 171027104 intron variant G/A snv 0.15 2
rs576674 1.000 0.080 13 32980164 intergenic variant G/A snv 0.69 2
rs6072275
TOP1 ; PLCG1-AS1
20 41115265 intron variant G/A snv 0.13 2
rs7118178
MTCH2
11 47637583 intron variant G/A snv 0.20 2
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs4237150
GLIS3
9 4290085 intron variant G/A;C;T snv 2
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs6113722
LINC00261
20 22576461 intron variant G/A;T snv 2
rs340878
PROX1-AS1 ; PROX1
1 213983706 intron variant G/C snv 0.63 2
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5