Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12680973
ADGRB1
8 142479537 non coding transcript exon variant T/C snv 0.84 0.85 1
rs9921412
PKD1L3
16 71954207 missense variant C/T snv 0.79 0.72 1
rs7140
SPNS1 ; LAT
16 28984436 missense variant C/A snv 0.73 0.76 1
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 2
rs4821888
SYNGR1
22 39374592 missense variant A/G;T snv 0.71; 2.9E-05 1
rs28433345
SH2B1
16 28872006 non coding transcript exon variant T/C snv 0.69 0.68 1
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 1
rs2303690
ELSPBP1
19 48022250 missense variant G/A;C snv 0.62 1
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 3
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs2955280
LRPPRC
2 43889697 intron variant C/A;G;T snv 0.59 1
rs3858954
SAXO2
15 82265693 missense variant G/A;C snv 0.59 1
rs889169
NPAS1 ; TMEM160
19 47045420 synonymous variant G/A snv 0.56 0.49 1
rs11130
NDE1 ; MYH11
1.000 0.040 16 15724453 3 prime UTR variant G/A;C snv 0.56; 4.0E-06 2
rs2072490
MAST3
19 18146940 synonymous variant C/G;T snv 0.53 1
rs1614887
BTN2A2
6 26392793 synonymous variant G/A snv 0.53 0.63 2
rs1108842
GNL3 ; PBRM1
3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 2
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs3754970
LOC101929512 ; TANK
2 161235325 intron variant T/A;C;G snv 2.7E-05; 0.48 1
rs11884495
TANK
2 161203458 intron variant A/T snv 0.48 0.43 1
rs7313259
ATF7IP
12 14475839 intron variant C/T snv 0.47 0.42 1
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs133383
PHETA2
22 42077599 synonymous variant C/T snv 0.44 0.35 1
rs2428507
HLA-L ; HCG17
6 30261529 intron variant A/G;T snv 0.44; 4.0E-05 1
rs2731664
GRK6
5 177432847 intron variant C/A;T snv 0.44; 3.9E-05 1