Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 4
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 3
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 3
rs1426371
LOC105369965 ; WSCD2
1.000 0.040 12 108236003 intron variant G/A snv 0.20 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs353547
TWF2
0.925 0.080 3 52234850 intron variant T/C snv 0.64 3
rs4684833 1.000 0.040 3 11990245 intergenic variant C/T snv 0.79 2
rs483143 0.925 0.080 6 27878966 intergenic variant G/C snv 0.13 2
rs80533 1.000 0.040 22 40689965 intergenic variant A/G snv 0.81 2
rs62064641
ARHGAP27
1.000 0.040 17 45411426 intron variant T/C snv 0.14 2
rs12765002
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875591 intron variant C/T snv 0.24 2
rs56133711
BDNF
1.000 0.040 11 27701787 intron variant G/A snv 0.19 2
rs10507274
C12orf49
1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 2
rs1248860
CADM2
1.000 0.040 3 84966628 intron variant G/A snv 0.56 2
rs76508707
CADM2
1.000 0.040 3 85347899 intron variant C/T snv 0.43 2
rs9854869
CADM2
1.000 0.040 3 85371574 intron variant C/A snv 0.17 2
rs6478623
DENND1A
1.000 0.040 9 123552844 intron variant T/G snv 0.36 2