Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 4
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 4
rs6741751
TRPM8
0.925 0.040 2 233919016 intron variant G/A snv 7.8E-02 3
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv 2
rs11759769
FHL5
1.000 0.040 6 96617336 downstream gene variant G/A snv 0.18 2
rs4379368
SUGCT
0.925 0.040 7 40426601 intron variant C/T snv 0.12 2
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 2
rs10915437 1.000 0.040 1 4122946 intergenic variant A/G snv 0.29 1
rs9490306 1.000 0.040 6 121495733 intergenic variant C/A snv 0.15 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs488884
LINC02109 ; LOC107986410
1.000 0.040 5 29040014 intron variant T/G snv 0.55 1
rs6790925
LOC101927995 ; LOC105377013
0.925 0.040 3 30438593 intergenic variant C/G;T snv 1
rs10504861
LOC105375630 ; LOC105375629
0.925 0.040 8 88535703 intron variant C/T snv 0.23 1
rs1835740
LOC105375655 ; LOC101927066
0.882 0.040 8 97154685 intergenic variant T/C snv 0.75 1
rs2274316
MEF2D
0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54 1
rs2651899
PRDM16 ; LOC105378606
0.882 0.040 1 3167148 intron variant T/A;C snv 1
rs17301853
RABGAP1L
1.000 0.040 1 174583673 intron variant C/T snv 0.12 1
rs7075426
WAPL
1.000 0.040 10 86456645 intron variant G/A snv 0.48 1