Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11935767
H2AZ1-DT
4 100093652 intron variant A/G snv 0.24 1
rs17882802
CHUK
10 100223656 intron variant G/A snv 0.30 1
rs112241539
CASTOR3
7 100249614 intron variant C/T snv 0.16 1
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 2
rs2679894
TGFBRAP1
2 105254322 upstream gene variant A/G snv 0.43 2
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 1
rs10156597
LINC01505
9 106179228 intron variant A/T snv 0.36 1
rs2519673 7 106354280 intergenic variant G/A;T snv 1
rs17153527 7 106855364 intergenic variant T/C snv 9.3E-02 1
rs77100210
YBX3 ; LOC112268104
12 10723329 upstream gene variant A/C;T snv 3.4E-02 1
rs6975557
NRCAM
7 108332853 intron variant A/G snv 0.29 1
rs12211124
SYCP2L
6 10886352 intron variant T/C snv 0.31 1
rs9358956
SYCP2L
6 10887020 5 prime UTR variant G/C;T snv 1
rs6899676
SYCP2L
6 10895027 intron variant A/G snv 0.21 2
rs2153157
SYCP2L
6 10897255 intron variant G/A snv 0.55 1
rs9393800
SYCP2L ; LOC101928191
6 10951504 intron variant A/G snv 0.20 2
rs12196873
MFSD4B
6 111276855 3 prime UTR variant A/C snv 0.10 1
rs7852169
PTGR1 ; ZNF483
9 111556114 intron variant C/G snv 0.15 2
rs7333181 1.000 0.040 13 111568950 intergenic variant G/A snv 0.11 1
rs2921759 8 116898565 intergenic variant T/C snv 0.10 1
rs10934420
LOC107986022
3 117833264 intron variant T/C snv 0.44 1
rs1029285
LOC105371084 ; GSPT1
16 11893261 intron variant G/A snv 0.43 1
rs10852344 16 11923062 upstream gene variant C/T snv 0.43 1
rs7137869
LOC105370027
12 119551841 intron variant A/G snv 0.19 1