Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 6
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs10445937 2 60410521 intron variant G/A snv 0.39 3
rs12464462 2 60409281 intron variant A/G;T snv 0.39 3
rs12476132 2 60412769 intron variant G/A snv 0.34 3
rs13009393 2 60406229 intron variant G/A snv 0.33 3
rs243063 2 60395764 intron variant A/T snv 0.35 3
rs243066 2 60394631 intron variant A/G snv 0.29 3
rs243067 2 60394508 intron variant G/C;T snv 3
rs243080
MIR4432 ; MIR4432HG
2 60387437 non coding transcript exon variant G/A snv 0.48 0.41 3
rs13027161
MIR4432HG
2 60380593 intron variant T/C snv 0.29 3
rs1553934
MIR4432HG
2 60382761 intron variant G/C;T snv 3
rs173373
MIR4432HG
2 60378784 intron variant C/T snv 0.33 3
rs2137281
MIR4432HG
2 60384873 non coding transcript exon variant C/T snv 0.29 3
rs2137283
MIR4432HG
2 60385322 non coding transcript exon variant C/A snv 0.30 3
rs243027
MIR4432HG
2 60379872 intron variant T/A;G snv 3
rs243029
MIR4432HG
2 60379519 intron variant C/T snv 0.33 3
rs243030
MIR4432HG
2 60379436 intron variant C/T snv 0.33 3
rs243032
MIR4432HG
2 60376815 intron variant G/A snv 0.33 3
rs243076
MIR4432HG
2 60390428 intron variant G/A snv 0.35 3