Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 2
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 3
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 2
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 1
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs12285364
SORL1
1.000 0.080 11 121522517 intron variant C/T snv 6.7E-02 1
rs12385797 11 106465562 upstream gene variant C/A snv 6.4E-02 1
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs1280 3 170995501 intron variant T/C snv 0.20 2
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs13100723
ARHGEF3
3 56764467 intron variant C/T snv 7.0E-02 1
rs13179048
LOC101929710 ; MIR583HG
5 96207022 intron variant C/A snv 0.23 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs13427272
CTNNA2
2 80058810 intron variant G/A snv 5.4E-02 1
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 1