Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs3812049
SLC12A2 ; LINC01184
5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs149290349
ZFP36L2
2 43224818 missense variant G/A;T snv 6.7E-02 3
rs61387190
SMG9
19 43756777 upstream gene variant C/A;T snv 3
rs10087240
PVT1
8 128000328 intron variant C/G;T snv 2
rs1822534 3 12225304 intergenic variant A/G;T snv 2
rs552599526
KLF3
4 38675391 intron variant C/-;CC;CCC;CCCC;CCCCC;CCCCCC delins 2
rs58106596 2 231714669 downstream gene variant G/A;C snv 2
rs658349
TBC1D1
4 38135732 intron variant C/G;T snv 2
rs66561220
LOC107984129 ; APOLD1 ; LOC105369663
12 12725831 upstream gene variant T/C;G snv 2
rs713909
CBX7
22 39136415 non coding transcript exon variant G/A;C;T snv 2
rs7192652
NLRC5
16 57041268 intron variant A/C;G snv 2
rs11077815
UBE2O
17 76393809 intron variant T/C;G snv 1
rs112158604 1 150724317 upstream gene variant GCTTCTGCA/- delins 1
rs113678689
RBMS1
2 160450317 intron variant G/C;T snv 1
rs113924863 6 32615369 regulatory region variant C/T snv 1
rs11779535 8 100376055 downstream gene variant G/A;C;T snv 1
rs12504282
ANTXR2
1.000 0.040 4 80005847 intron variant C/G;T snv 1
rs12716977
ITGAL
16 30471482 upstream gene variant T/A;C snv 1
rs12733073
PTPRC
1 198710886 intron variant G/A;C snv 1
rs12981683
ARRDC2
19 18003191 intron variant C/G;T snv 1
rs13230583 7 150620190 intergenic variant T/A;C snv 1
rs140508453
SLC35D1
1 67015161 intron variant AAAAAAAA/-;AA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAAA;AAAAAAAAAA delins 1
rs2022542
TSBP1-AS1 ; TSBP1
6 32318908 intron variant A/G;T snv 1
rs34233420
IKZF3
17 39848677 intron variant ATTT/- delins 1