Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 6
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5