Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 1
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 1
rs809871
LOC105374986
6 26256298 downstream gene variant C/G;T snv 1
rs9883204
ADCY5
3 123377973 intron variant T/A;C snv 1
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 1
rs17064002 13 42996665 upstream gene variant C/T snv 1.8E-02 1
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 1
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 1
rs17138114 6 4379277 intron variant A/G snv 0.10 1
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 3
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 1
rs3107997
LOC105372047 ; LOC105372046
18 30340278 intron variant C/T snv 0.21 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs12461110
NLRP11
19 55809297 missense variant G/A snv 0.32 0.26 1
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 1
rs7849941
LOC107987088
9 85130318 intergenic variant A/T snv 0.27 1
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 1