Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs2093816
LINC02341
0.882 13 42471900 intron variant C/T snv 0.47 4
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7