Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7777102 7 73643687 intergenic variant A/G;T snv 5
rs2420371
F5
1 169522317 intron variant G/A snv 0.95 4
rs1160297
LOC105369165
2 53010182 intergenic variant G/C snv 0.69 3
rs1397048
OR9G1
11 56698623 upstream gene variant C/T snv 0.54 3
rs1413885
DNAJC6
1 65349976 intron variant C/T snv 0.72 3
rs2025096
GSS
20 34952197 5 prime UTR variant G/A snv 0.19 3
rs2295888
EDEM2 ; MMP24-AS1-EDEM2
20 35135060 intron variant A/G snv 0.14 3
rs2425068
CPNE1
20 35626801 splice acceptor variant T/C snv 6.2E-02 4.7E-02 3
rs4133289
LINC02819
1 159484147 downstream gene variant C/T snv 0.16 3
rs6058227
UQCC1
20 35308144 intron variant C/T snv 0.15 3
rs6087685
PROCR ; MMP24-AS1-EDEM2
20 35189809 intron variant G/C snv 0.40 3
rs6088735
MMP24-AS1-EDEM2
20 35157873 intergenic variant C/T snv 0.25 3
rs6120993
FER1L4
20 35597239 intron variant G/T snv 0.24 3
rs7159841
MDGA2
14 47394632 intron variant C/T snv 0.72 3
rs819131 20 34320043 intergenic variant G/A snv 0.87 3
rs1011019
ERCC3
2 127279984 intron variant A/G;T snv 0.75 2
rs1018503
NCOA6
20 34737712 intron variant T/A;G snv 2
rs1019842
MYO7B
2 127547621 intron variant T/C snv 0.86 2
rs1033797
MMP24-AS1-EDEM2 ; EDEM2
20 35131884 intron variant T/C snv 0.27 2
rs1033799
EDEM2 ; MMP24-AS1-EDEM2
20 35132230 intron variant C/A snv 0.17 2
rs1040552 20 33861523 regulatory region variant A/G snv 0.19 2
rs10485508
TRPC4AP
20 35017295 intron variant C/T snv 8.0E-02 2
rs10496661
MAP3K2
2 127332568 intron variant G/T snv 0.24 2
rs1058003
TRPC4AP ; MYH7B
20 35002614 3 prime UTR variant G/A snv 0.58 2
rs10803588
LOC105373609 ; MYO7B
2 127570800 intron variant C/T snv 0.37 2