Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs35809595
ARID5B
10 62072169 intron variant G/A snv 0.33 1
rs71313931
ARVCF
22 19972661 intron variant C/G snv 0.23 1
rs1412710
COL12A1
6 75127487 intron variant T/A;C snv 1
rs7032489
COL5A1
9 134667929 intron variant C/G;T snv 1
rs8133436
COL6A2
21 46099621 intron variant T/A;C snv 1
rs1309531
CWC27
5 65010484 intron variant A/T snv 0.42 1
rs8030753
FBN1
15 48509738 intron variant C/T snv 0.15 1
rs6445046
FNDC3B
3 172215462 intron variant G/A;T snv 1
rs7026684
GLIS3
9 4215308 intron variant G/A snv 0.39 1
rs11111869
GLT8D2
12 104008707 intron variant G/A snv 0.13 1
rs1931656
LINC02542
6 81900471 intron variant A/T snv 0.53 1
rs1536478
LOC100506532
9 134540402 intron variant G/A;C snv 1
rs4965359
LOC105371026 ; LRRK1
15 101045131 intron variant G/A snv 0.34 1
rs9361886
LOC107986617 ; LINC02542
6 82068785 intron variant T/C snv 0.45 1
rs3808520
LOXL2
8 23307260 intron variant G/C snv 0.17 1