Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs347412
DGKH
1.000 0.080 13 42212544 intron variant A/G;T snv 3
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs4954192
CCNT2-AS1 ; ACMSD
1.000 0.080 2 134875411 intron variant C/T snv 0.52 3
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs7625643
ZBTB38
0.925 0.080 3 141431184 intron variant A/G snv 0.51 3
rs7626218
TBL1XR1
0.925 0.080 3 177134250 intron variant A/T snv 0.41 3
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs7918084
EIF2S2P3
1.000 0.080 10 92669710 non coding transcript exon variant C/T snv 0.60 3
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34 3
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs10074523
KIF3A
1.000 0.080 5 132724891 intron variant C/A snv 0.62 2
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv 2
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs1017494 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 2
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 2
rs10187276 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 2
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs10836538
PRR5L
0.925 0.080 11 36343703 intron variant G/T snv 0.30 2
rs10965947
LOC101929563
1.000 0.080 9 23588585 intron variant C/T snv 0.38 2
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2