Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2206271
TFAP2B
6 50818295 upstream gene variant T/A snv 0.32 3
rs246185
MIR193BHG
16 14301575 intron variant T/C snv 0.34 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 3
rs4929923
TRIM66
11 8617653 3 prime UTR variant T/C snv 0.59 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 3
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64 2
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 2
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 2
rs1172955 10 96117563 downstream gene variant T/A snv 0.60 2
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 2
rs12462111
NTN5 ; SEC1P
19 48668049 intron variant C/T snv 0.33 2
rs1285245
LOC102723961 ; LINC01977
17 79823090 non coding transcript exon variant G/C snv 0.45 2
rs13064915 3 137402401 intergenic variant T/C snv 0.42 2
rs1351623
TACR3
4 103666820 intron variant C/T snv 0.36 2
rs1361108
CENPW
6 126446454 intron variant C/T snv 0.44 2
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs16937956
STK33
11 8382954 regulatory region variant A/G snv 0.35 2
rs16938437
PHF21A
11 46031024 intron variant C/T snv 0.13 2
rs17266097
SATB2
2 199410486 intron variant C/T snv 0.29 2
rs1861072
UNC80
2 209986910 intron variant T/C snv 0.34 2
rs2003476
CRTC1
19 18695858 intron variant T/C snv 0.53 2
rs2267958
DNM1
9 128253000 non coding transcript exon variant G/A snv 0.38 2