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
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs13001243 0.882 0.040 2 234306004 regulatory region variant G/A snv 7.5E-02 3
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs201048567 0.882 0.040 7 125615031 intergenic variant CA/- delins 1.0E-05 3
rs2997119 0.882 0.040 13 55819766 intergenic variant A/G snv 0.52 3
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 3
rs56196471 0.882 0.040 4 178642661 intergenic variant G/A snv 2.9E-02 3
rs62482377 0.882 0.040 7 156250946 intergenic variant G/C snv 0.10 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs77867520 0.882 0.040 4 11186225 intergenic variant C/T snv 7.2E-02 3
rs9354352 0.882 0.040 6 65986379 intergenic variant T/C snv 0.42 3
rs56031956
ACTL7A
0.882 0.040 9 108863349 missense variant C/G snv 2.3E-02 2.2E-02 3
rs146330533
ARHGEF10L
0.882 0.040 1 17669971 intron variant G/A snv 1.2E-02 3
rs11125080
ATP6V1E2
0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs188839109
C11orf21 ; TSPAN32
0.882 0.040 11 2301859 start lost C/T snv 1.0E-02 9.6E-03 3
rs4800149
CABLES1
0.882 0.040 18 23164290 intron variant C/A snv 0.80 3
rs12052005
CCDC102B
0.882 0.040 18 68832311 intron variant G/C;T snv 3
rs34486957
CCDC175
0.882 0.040 14 59578879 upstream gene variant C/T snv 0.24 3
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv 3
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3