Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10086568 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 2
rs10100356
CCDC26
8 129613918 intron variant G/A snv 0.22 1
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36 2
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs1025688
MAPK4
18 50621506 intron variant G/A snv 0.35 3
rs10265538 7 20502242 intergenic variant T/C snv 0.20 2
rs10283564
INSL6 ; JAK2
9 5075628 intron variant C/G snv 0.23 2
rs1032726
CD200R1
3 112967228 intron variant T/C snv 0.46 2
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs10401672 19 33269055 regulatory region variant C/T snv 0.30 1
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2
rs10542411 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 2
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs10852622
ZFPM1
16 88490472 intron variant A/G snv 0.35 2
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs10893844 11 128315955 regulatory region variant G/C snv 0.36 2
rs10995240
LOC105378327 ; ZNF365
10 62628871 intron variant G/C snv 0.29 2
rs11018874
NAALAD2
11 90142269 intron variant G/A snv 9.7E-02 1