Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7