Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs11190604
HIF1AN
10 100542700 intron variant A/G snv 0.19 2
rs994988 6 103351171 intergenic variant C/T snv 0.44 2
rs10220265 13 103397233 downstream gene variant G/A snv 0.28 1
rs9586177 13 103407580 intergenic variant C/T snv 0.21 1
rs9586178 13 103407668 intergenic variant G/T snv 0.20 1
rs9586179 13 103407737 intergenic variant T/C snv 0.21 1
rs9586180 13 103407783 intergenic variant T/C;G snv 1
rs7490068 13 103408045 intergenic variant G/A;C snv 1
rs1330767 13 103408241 intergenic variant C/T snv 0.21 1
rs2210152 13 103409236 intergenic variant T/C snv 0.22 1
rs2210153 13 103409291 intergenic variant G/A snv 0.22 1
rs9368446
SYCP2L
6 10891987 intron variant G/A snv 0.26 1
rs9366664
SYCP2L
6 10892266 intron variant T/C snv 0.38 1
rs946350
SYCP2L
6 10892720 intron variant G/A;C snv 1
rs9368452
SYCP2L
6 10893446 intron variant G/C;T snv 1
rs9368453
SYCP2L
6 10894022 intron variant G/A snv 0.29 0.27 1
rs6456745
SYCP2L
6 10894035 intron variant A/G snv 0.36 0.38 1
rs9357021
SYCP2L
6 10905921 intron variant A/G snv 0.23 1
rs9366669
SYCP2L
6 10908636 intron variant G/A snv 0.19 1
rs6928281
SYCP2L
6 10908684 intron variant G/T snv 0.70 1
rs9467921
SYCP2L
6 10910386 intron variant C/G;T snv 1
rs4713044
SYCP2L
6 10911049 intron variant G/A snv 0.68 1
rs9461310
SYCP2L
6 10919963 intron variant A/G snv 0.31 1
rs12190237
SYCP2L
6 10922405 intron variant G/A snv 0.24 1