Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1336708
FGF14 ; FGF14-IT1 ; LOC107984615
13 102312653 intron variant A/G snv 0.28 1
rs2771051 9 117525430 intergenic variant G/A;T snv 1
rs1985317 9 117530056 intergenic variant C/T snv 0.48 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2282015
LINC02641
1.000 0.040 10 123462521 intron variant T/G snv 0.39 1
rs1799810
PROC
1.000 0.040 2 127418464 5 prime UTR variant A/T snv 0.38 0.44 2
rs664910
MGLL
3 127755187 intron variant G/A snv 0.63 1
rs12541254
DLC1
8 13121891 intron variant G/A snv 0.37 1
rs1364505
PLXNA4
7 132345252 intron variant G/A snv 0.33 1
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs8176732
ABO
9 133256916 intron variant A/G snv 0.25 3
rs8176728
ABO
9 133257174 intron variant G/C;T snv 3
rs2073825
ABO
9 133257320 intron variant A/T snv 0.25 3
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv 3
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 3
rs8176717
ABO
9 133257647 intron variant G/T snv 0.26 3
rs8176714
ABO
9 133257791 intron variant G/A snv 0.26 4
rs641959
ABO
9 133258308 intron variant A/C snv 0.29 4
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs514708
ABO
9 133258352 intron variant C/T snv 0.29 4
rs517414
ABO
9 133258643 intron variant G/A snv 0.26 3
rs638756
ABO
9 133259081 intron variant A/C snv 0.28 2
rs626035
ABO
9 133259603 intron variant T/G snv 0.28 4
rs547643
ABO
9 133259656 intron variant C/T snv 0.27 3
rs625593
ABO
9 133259705 intron variant G/A;T snv 2