Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11053550
LOC112268091 ; LOC102724020
12 10019754 intron variant T/C snv 0.15 1
rs893245 2 100198431 regulatory region variant C/T snv 0.55 1
rs6542920
LINC01104
2 100228626 intron variant A/G snv 0.64 1
rs4851273
LINC01104
2 100231859 intron variant A/G snv 0.64 1
rs4437940 10 10023280 intergenic variant G/A;T snv 1
rs7597861
LINC01104
2 100236725 intron variant G/A snv 0.65 1
rs12474386
LINC01104
2 100240555 intron variant G/A snv 0.46 1
rs6739695
LINC01104
2 100243160 intron variant A/C;G snv 1
rs10865036
LINC01104
2 100244133 intron variant T/C snv 0.65 1
rs2309811
LINC01104
2 100245897 intron variant A/G snv 0.65 1
rs6737502
LINC01104
2 100246441 intron variant C/T snv 0.65 1
rs6542921
LINC01104
2 100248036 intron variant C/A snv 0.64 1
rs4851274 2 100254400 downstream gene variant T/C snv 0.65 1
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs10783130 1 100341341 upstream gene variant C/G snv 0.21 1
rs11166439 1 100342730 upstream gene variant G/C;T snv 1
rs537783 11 100377590 intergenic variant C/A snv 0.16 1
rs1145412 11 100378042 intergenic variant T/C snv 0.17 1
rs10894847 11 100385044 intergenic variant G/T snv 0.17 1
rs9386144
LOC102724406 ; SIM1
6 100425381 intron variant T/C snv 0.17 1
rs3778033
LOC102724406 ; SIM1
6 100427640 intron variant T/C snv 0.19 1
rs12769144
DPCD
10 101609797 downstream gene variant A/C snv 7.6E-02 1
rs985375
ZPLD1
3 102348402 intron variant G/A snv 0.31 1
rs10820660
OR13F1
9 104503209 upstream gene variant A/G snv 0.13 1
rs17812021
CHST11
12 104534885 intron variant C/G snv 5.0E-02 1