Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59876823
PCCA-DT
13 100082270 intron variant C/A snv 0.10 2
rs10958852
PTPRD
9 10060843 intron variant C/T snv 4.5E-04 2
rs182466621
LOC105375310
2 100730839 intergenic variant G/A;T snv 2
rs140386998 X 100959983 downstream gene variant C/T snv 3.7E-02 2
rs60866311
NPAS2 ; NPAS2-AS1
2 100975599 non coding transcript exon variant T/G snv 4.1E-02 7.2E-02 2
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 3
rs3862030
SUFU
10 102567827 intron variant A/G snv 0.45 2
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46 3
rs71417845 14 103210903 downstream gene variant C/G snv 1.7E-02 2
rs41427747
LINC02503
4 103999322 intron variant G/T snv 5.6E-02 2
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs10991437
CT70
9 104973639 intron variant C/A snv 9.0E-02 2
rs58376408 16 10504450 regulatory region variant C/G snv 6.5E-02 2
rs144529734
LOC107984266
10 105647558 intergenic variant G/T snv 1.4E-02 2
rs9408815
LINC01505
9 106128240 intron variant C/G snv 0.20 2
rs9409082
LINC01505
9 106138768 intron variant C/T snv 0.20 2
rs670752
BBX
3 107594133 intron variant G/A;T snv 2
rs13271456
LOC102723313 ; PINX1
8 10767736 intron variant G/A snv 2.7E-02 2
rs6437740
BBX
3 107746970 intron variant T/C snv 0.25 1
rs12710258
CARM1
19 10879653 intron variant C/T snv 0.16 2
rs10041657
FER
5 108816727 intron variant G/A snv 0.23 2
rs78553789
MYO16
13 108904171 intron variant T/C snv 2.3E-02 2
rs848353 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 1
rs117178387
AMD1 ; CDK19
6 110815877 non coding transcript exon variant T/C snv 3.2E-02 2
rs150400940
LOC105378486 ; LOC107984268
10 112050671 intergenic variant C/T snv 3.0E-02 2