Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs300774 0.925 0.040 2 112496 intergenic variant A/C;T snv 1
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs8283
ATF6B ; TNXB
0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 4
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 3
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 2
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 2
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 2
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 2
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 2
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 2
rs1002424
PRKAA1
1.000 0.040 5 40767295 intron variant A/G snv 0.31 1
rs10226475
MAD1L1
1.000 0.040 7 2186527 intron variant A/G snv 0.34 1
rs10498146 1.000 0.040 2 222987318 intergenic variant A/G snv 6.2E-02 1
rs10503256
CSMD1
1.000 0.040 8 4356657 intron variant A/G snv 0.57 1
rs10503899
NRG1 ; NRG1-IT1
1.000 0.040 8 32089718 intron variant A/G snv 0.33 1
rs1064627
FLOT1
1.000 0.040 6 30730764 non coding transcript exon variant A/G snv 0.17 0.19 1
rs10791946
ENPP7P7
1.000 0.040 11 67820541 intron variant A/G snv 0.41 1