Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs12459419
CD33
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs2027605
BACH1
1.000 0.120 21 29354452 intron variant A/G snv 0.48 2
rs4846913
GALNT2
1.000 0.120 1 230158968 intron variant C/A;T snv 2
rs927292
ZFP36L1
1.000 0.120 14 68792124 intron variant C/G snv 0.68 2
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs4360494
SF3A3
0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs2074585
IQGAP1
0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs112329286
SYNE2
1.000 0.080 14 63773159 intron variant -/ATTT delins 0.24 4
rs1169299
HNF1A
1.000 0.080 12 120991391 intron variant T/C snv 0.43 4
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs7606173
BCL11A
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 4
rs10011838 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 3
rs332388
SLC25A26
1.000 0.080 3 66361431 intron variant T/C snv 0.55 3
rs428073
TAOK3
1.000 0.080 12 118244946 missense variant C/G;T snv 0.72 3