Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
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
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 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
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
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5