Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs56364076
CAVIN1
1.000 0.040 17 42413017 intron variant C/T snv 0.58 1
rs963986
CAVIN1
1.000 0.040 17 42409561 intron variant G/C snv 0.15 1
rs130067
CCHCR1
0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21 1
rs1576
CCHCR1
1.000 0.040 6 31142614 missense variant G/A;C snv 4.0E-06; 0.28 1
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs118086960
CFL1
1.000 0.040 11 65825973 intron variant A/T snv 0.62 1
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 1
rs34394770
COG6
1.000 0.040 13 39759232 intron variant T/C snv 0.29 1
rs36207871
CS
1.000 0.040 12 56290713 intron variant AGGAA/- delins 0.79 1
rs9987128
CSMD1
1.000 0.040 8 3122601 intron variant A/G snv 0.17 1
rs11795343
DDX58
1.000 0.040 9 32523739 intron variant T/C snv 0.41 1
rs2700987
ELMO1
1.000 0.040 7 37346633 intron variant C/A snv 0.60 1
rs2724013
ELMO1
1.000 0.040 7 37349706 intron variant G/A;T snv 1
rs2076346
ELOA-AS1 ; ELOA
1.000 0.040 1 23757159 intron variant T/C snv 0.27 0.21 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 1
rs6590334
ETS1
1.000 0.040 11 128533313 intron variant T/C snv 0.60 1
rs2476847
EXOC2
1.000 0.040 6 549390 intron variant C/T snv 0.44 1
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 1
rs6517178
GART
1.000 0.040 21 33516314 intron variant T/A;C;G snv 1
rs6444895
GPR160
1.000 0.040 3 170083870 intron variant G/A snv 0.43 1
rs9513593
GPR183 ; UBAC2
1.000 0.040 13 99298006 intron variant G/A snv 0.71 1