Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13412535
SERPINE2
2 224010157 intron variant G/A snv 0.17 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs34651
TNPO1
1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 4
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs11601507
TRIM5
1.000 0.040 11 5679844 missense variant C/A;T snv 9.3E-02; 4.0E-06 3
rs11734132 4 6889792 intergenic variant G/C snv 0.17 3
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 3
rs12445050
PLCG2
16 81837364 intron variant C/T snv 9.6E-02 3
rs139141690
CUX1
7 101856650 intron variant G/A snv 2.2E-03 3
rs17116384
ZBTB16
11 114110519 intron variant A/G snv 0.25 3
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 3
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3