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
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs2954031 8 125479491 intron 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
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 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
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 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
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 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
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5