Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs3132581
MUCL3 ; HCG21 ; SFTA2
0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs1715
ZNF615
0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs11756438
CEP85L
0.925 0.040 6 118672469 intron variant C/A snv 0.42 3
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs10492664 0.925 0.040 13 108163877 intergenic variant C/A;T snv 2
rs10956838 1.000 0.040 8 92392214 intergenic variant A/C snv 0.28 2
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs1334489 0.925 0.040 6 118318224 downstream gene variant T/A snv 0.37 2
rs16998572 0.925 0.040 20 53935345 upstream gene variant G/C snv 0.11 2
rs4259397 0.925 0.040 8 92354062 upstream gene variant G/A;T snv 2
rs4858253 0.925 0.040 3 20687599 intron variant C/T snv 0.33 2
rs7094182 0.925 0.120 10 8484656 intergenic variant G/A;C snv 2
rs74760947 0.925 0.040 8 34495092 intergenic variant A/G snv 3.1E-02 2
rs797267 0.925 0.040 12 89373460 intron variant A/G snv 0.28 2