Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1536482 1.000 0.040 9 134548682 upstream gene variant G/A snv 0.36 3
rs12448211 16 88296907 intron variant G/A snv 0.56 2
rs28687756 16 88295322 intron variant T/G snv 6.5E-04 2
rs3118520 9 134549749 upstream gene variant A/G snv 0.49 2
rs4792535 17 14661813 intergenic variant C/T snv 0.45 2
rs4938174 11 111042516 upstream gene variant G/A snv 0.31 2
rs7040970 9 136964561 upstream gene variant T/C snv 0.44 2
rs10161679 13 22669506 intergenic variant G/A;C snv 1
rs13024279 2 234563951 intergenic variant A/G snv 0.47 1
rs16920206 10 64725315 intergenic variant T/C snv 2.3E-02 1
rs2106166 7 93039018 intergenic variant A/T snv 0.44 1
rs2419835 10 113536805 intergenic variant C/T snv 0.72 1
rs3094339 9 134019616 intergenic variant G/A;C snv 1
rs3132303 9 134552452 upstream gene variant C/G;T snv 1
rs35193497 16 88291215 intron variant T/G snv 0.57 1
rs66720556 9 13559718 intron variant T/A snv 0.20 1
rs7308752 12 91133404 regulatory region variant A/G snv 0.25 1
rs35028368
ADAMTS2
5 179244141 intron variant -/A delins 1
rs10064391
ADAMTS6
5 65390832 intron variant A/G snv 0.37 1
rs10471310
ADAMTS6
5 65253134 intron variant C/T snv 0.37 1
rs4843040
ADAMTS7P4
15 85295405 intron variant C/T snv 0.32 1
rs56009602
ADAMTS8
11 130419717 intron variant C/A;T snv 2
rs35809595
ARID5B
10 62072169 intron variant G/A snv 0.33 1
rs71313931
ARVCF
22 19972661 intron variant C/G snv 0.23 1
rs752092
CHSY1
15 101241729 intron variant A/G snv 0.43 2