Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191732
NEURL1
1.000 0.040 10 103572004 intron variant G/A snv 0.14 1
rs12887734
COA8 ; KLC1
1.000 0.040 14 103580497 intron variant G/T snv 0.26 2
rs35229468
KLC1 ; COA8
1.000 0.040 14 103585720 intron variant C/T snv 0.25 2
rs10895475 1.000 0.040 11 103593113 intergenic variant C/A;T snv 1
rs9879311
ATP2B2
1.000 0.040 3 10373659 intron variant C/A;T snv 2
rs17292804
PPP1R13B
1.000 0.040 14 103738786 synonymous variant G/A snv 8.0E-02 8.5E-02 2
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 2
rs8009147
PPP1R13B
1.000 0.040 14 103798325 intron variant A/G;T snv 2
rs10083370
LINC00637 ; PPP1R13B
1.000 0.040 14 103847845 intron variant G/A snv 0.55 1
rs12543645
MSRA
1.000 0.040 8 10388815 intron variant G/A;C snv 1
rs12541491
MSRA
1.000 0.040 8 10392538 intron variant C/A;G;T snv 1
rs112973353 1.000 0.040 14 104071343 intergenic variant C/T snv 7.3E-02 1
rs950394 1.000 0.040 2 104353789 intergenic variant G/A snv 0.16 1
rs62152284 1.000 0.040 2 104367929 intergenic variant C/G;T snv 1
rs2905627
CXXC4-AS1
1.000 0.040 4 104528928 intron variant C/A;T snv 1
rs313327
CHST11
1.000 0.040 12 104580243 intron variant C/T snv 0.75 1
rs11192193
SORCS3
1.000 0.040 10 104809495 intron variant A/G snv 0.52 2
rs7776707
LINC01004 ; KMT2E
1.000 0.040 7 104965083 intron variant C/A snv 0.31 2
rs314272
LIN28B
1.000 0.040 6 105014129 intron variant G/A;C snv 1
rs160593
LIN28B
1.000 0.040 6 105018457 intron variant G/A snv 0.50 1
rs1460583
ZFPM2
1.000 0.040 8 105096365 intron variant T/C snv 0.26 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs41563
SRPK2
1.000 0.040 7 105212207 intron variant G/A;C snv 2
rs7674220
TET2-AS1 ; TET2
1.000 0.040 4 105227601 intron variant G/A;C snv 2
rs4580973
SRPK2
1.000 0.040 7 105263212 intron variant A/G snv 0.45 2