Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs1490384 6 126530014 intron variant C/G;T snv 3
rs16917237
BDNF ; BDNF-AS
11 27680836 intron variant G/T snv 0.16 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 3
rs246185
MIR193BHG
16 14301575 intron variant T/C snv 0.34 3
rs707938
MSH5-SAPCD1 ; MSH5 ; SAPCD1
6 31761582 synonymous variant A/G snv 0.38 0.44 3
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 3
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs2206271
TFAP2B
6 50818295 upstream gene variant T/A snv 0.32 3
rs4929923
TRIM66
11 8617653 3 prime UTR variant T/C snv 0.59 3
rs1172955 10 96117563 downstream gene variant T/A snv 0.60 2
rs13064915 3 137402401 intergenic variant T/C snv 0.42 2
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs3893384 1.000 0.040 15 79680713 regulatory region variant C/T snv 0.50 2
rs57149692 16 30130700 regulatory region variant G/C snv 0.46 2
rs6087709 20 35430145 upstream gene variant C/G snv 0.25 2
rs7141210 14 100716133 regulatory region variant T/C snv 0.55 2
rs7306275 12 49856328 upstream gene variant G/A snv 0.29 2
rs7846385 8 77247943 intergenic variant T/C snv 0.23 2
rs815715 3 61278410 intergenic variant C/G snv 0.54 2
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 2
rs3027009
ACKR1 ; CADM3-AS1
1 159204097 intron variant A/G snv 5.8E-02 2