Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12699921 7 17954871 intergenic variant G/A snv 0.40 1
rs194714 14 68828731 intergenic variant T/C snv 0.24 1
rs194741 14 68821715 intergenic variant A/G snv 0.24 1
rs2376015 1 65658091 intergenic variant A/G snv 0.43 1
rs2420915 10 121080764 regulatory region variant G/A snv 0.25 1
rs367677 14 68806373 intergenic variant A/G snv 0.25 1
rs4655582 1 65687680 regulatory region variant C/G snv 0.34 1
rs61542988 7 22842672 regulatory region variant C/T snv 0.35 1
rs72679199 4 154554097 upstream gene variant C/T snv 0.15 1
rs72681211 4 154558109 upstream gene variant T/A snv 0.17 1
rs7439150 4 154560389 upstream gene variant G/A snv 0.17 1
rs76289367 4 154625007 upstream gene variant T/G snv 0.13 1
rs9808651 21 39094542 intergenic variant G/A snv 0.21 1
rs4766897
ACAD10
12 111741667 intron variant T/A;C snv 1
rs56702977
CAPN3
15 42379110 intron variant G/A snv 0.16 1
rs8026198
CAPN3
15 42361263 intron variant A/C;T snv 1
rs11859517
CHD9
16 53147335 intron variant C/T snv 0.28 1
rs12598049
CHD9
16 53282942 intron variant A/G snv 0.28 1
rs6499550
CHD9
16 53308542 intron variant C/T snv 0.31 1
rs11864453
DHODH
16 72016581 non coding transcript exon variant C/T snv 0.39 1
rs2731439
DIP2B
12 50666567 intron variant C/T snv 0.28 1
rs2699429
DOK7
4 3478409 intron variant T/C snv 0.54 1
rs150768229
FGB
4 154567149 intron variant A/C snv 9.5E-03 1
rs2227401
FGB
4 154565229 3 prime UTR variant C/T snv 0.17 0.17 1
rs3138493
GADD45G ; LOC105376139
9 89604345 intron variant T/C snv 0.52 1