Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141252918
CCDC170
0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs4870888
FER1L6 ; FER1L6-AS2
0.882 0.040 8 124096736 intron variant T/C snv 0.39 4
rs9577511
GRTP1
0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs62173322
KLHL23
0.882 0.040 2 169754519 intron variant A/G snv 0.32 4
rs76371172
OTUD7A ; LOC105370753
0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs11004733
PCDH15
0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs149268645
WDR12 ; CARF
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs26318
COMMD10
0.925 0.040 5 116352208 intron variant C/T snv 0.99 3
rs17387100
PROM1
0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 3
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 3
rs111326206 1.000 0.040 3 142719589 intron variant T/C snv 7.9E-02 2
rs111367251 1.000 0.040 7 145271196 downstream gene variant C/G snv 7.8E-03 2
rs111625585 1.000 0.040 14 82337988 intergenic variant C/T snv 4.2E-02 2
rs113386487 1.000 0.040 10 13316583 downstream gene variant A/G;T snv 2
rs13137453 1.000 0.040 4 152986727 intergenic variant A/G snv 1.9E-02 2
rs17399603 1.000 0.040 3 101017295 regulatory region variant A/G snv 0.10 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs183414028 1.000 0.040 1 39976354 intergenic variant T/C snv 1.4E-05 2
rs186736781 1.000 0.040 2 239551396 intergenic variant C/T snv 6.9E-03 2
rs300774 0.925 0.040 2 112496 intergenic variant A/C;T snv 2
rs3858375 1.000 0.040 11 95344003 intergenic variant C/T snv 0.15 2
rs482039 1.000 0.040 1 190808437 intergenic variant C/T snv 9.1E-02 2
rs62199592 2 183858773 intergenic variant A/G snv 2.1E-02 2
rs62460873 1.000 0.040 7 85348650 intergenic variant T/C;G snv 7.8E-03 2
rs180697792
ABCA5
1.000 0.040 17 69298289 intron variant G/A snv 2