Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 1
rs10740995
CACNB2
10 18156159 intron variant G/A;T snv 1
rs10849891
KDM2B
12 121473799 intron variant T/A;G snv 1
rs112684153
MTRF1
13 41275595 intergenic variant T/C;G snv 1
rs113602013 18 60252477 intergenic variant G/A;C snv 1
rs11601694
C1QTNF4
11 47593023 intron variant C/A;T snv 1
rs11724647
LOC107984032 ; GUCY1A1
4 155725188 intron variant T/A;C snv 1
rs11767188
HIBADH
7 27532326 intron variant A/G;T snv 1
rs11770148
MAD1L1
7 1859811 intron variant A/G;T snv 1
rs11880800
CRTC1
19 18730347 intron variant C/A;G snv 1
rs12363917
ALG9
11 111793677 intron variant C/G;T snv 1
rs12731208
PHF13
1 6616425 intron variant T/A;C;G snv 1
rs12758407
HNRNPFP1
1 42041342 non coding transcript exon variant T/A;G snv 1
rs13021222 2 164191395 intron variant G/C;T snv 1
rs145158522
SORCS3
10 104870101 intron variant C/A;G;T snv 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 1
rs1877312
LINC01478
18 44514546 intron variant C/A;T snv 1
rs1962094
ARMC4
10 27963710 intron variant T/A;C snv 1
rs2011567
NDUFAF6
8 94959692 intron variant G/A;C snv 1
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs2288276
HOXB-AS3 ; HOXB5 ; HOXB3
17 48593060 intron variant G/A;C snv 1
rs2290769
UNC13D
17 75830325 intron variant G/A;C snv 4.9E-06; 0.18 1