Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs11545169
PSMD2
3 184302754 missense variant G/T snv 0.13 0.11 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs6119267
NOL4L-DT ; NOL4L
20 32576112 intron variant C/A;G snv 3
rs6731373
LOC107985892
2 68275912 intergenic variant G/A snv 0.29 3
rs6870983
TMEM161B-AS1
5 88401716 intron variant C/T snv 0.29 3
rs72829446
ATP1B2
17 7648805 intron variant C/T snv 6.5E-02 3
rs75757892
RREB1
6 7232156 intron variant C/T snv 0.12 3
rs7963801
SYT1
12 79291446 intron variant T/C snv 0.70 3
rs8067165
LOC105376799
17 8128618 upstream gene variant C/A;G;T snv 3
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10783018
LOC101928219 ; LINC02607
1 95782279 non coding transcript exon variant G/A snv 0.74 2
rs10858334
OLFM1
9 135097939 3 prime UTR variant C/A;G snv 9.4E-02 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10949662
PTPRN2
7 157741413 intron variant C/A;T snv 2
rs10954772
PURG
8 31006422 intron variant T/A;C snv 2
rs11076962
RBFOX1
16 5761366 intron variant T/C snv 0.25 2
rs1107960 14 54917622 intergenic variant T/A snv 0.42 2
rs115024193
LOC105377299 ; BMP2K
4 78793500 intron variant T/A snv 2.3E-02 2
rs11588857
LRRN2 ; LOC105371692
1 204617919 missense variant G/A;T snv 0.20; 8.0E-06 2
rs11714441
ADCY5
3 123440099 intron variant C/T snv 0.40 2