Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 3
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs2274465
KDM4A
1 43655886 intron variant C/G snv 0.27 2
rs3027009
ACKR1 ; CADM3-AS1
1 159204097 intron variant A/G snv 5.8E-02 2
rs630602
SSBP3
1 54263191 intron variant G/C snv 0.62 2
rs643428
SSBP3
1 54263185 intron variant C/G;T snv 2
rs66461782
ZRANB2-AS1 ; ZRANB2 ; MIR186
1 71067604 intron variant A/T snv 0.32 0.27 2
rs7553348
FPGT-TNNI3K ; TNNI3K ; LRRC53
1 74539383 intron variant G/A snv 0.42 2
rs100537
RXRG
1 165444407 intron variant A/G snv 0.60 1
rs1032728
SCMH1
1 41213894 intron variant A/T snv 0.17 1
rs1040070
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74512186 intron variant G/A;C snv 1
rs10789181
DNAJC6
1 65350884 intron variant A/G snv 0.72 1
rs10874340 1 82793397 intron variant G/A;T snv 1
rs10913213
PAPPA2
1 176594124 intron variant C/G snv 0.32 1
rs11165924
DPYD
1 97909892 intron variant A/G snv 0.23 1
rs113184243
ARID1A
1 26737891 intron variant G/T snv 5.8E-02 1
rs11578152 1 102111465 intergenic variant A/G;T snv 1
rs12040029
RPS6KC1
1 213278615 downstream gene variant C/T snv 0.11 1
rs17449243
EIF4G3
1 20847936 non coding transcript exon variant T/C snv 0.10 1
rs1973284
AKT3
1 243693379 intron variant A/G;T snv 1
rs2194899
RXRG
1.000 0.160 1 165441548 intron variant A/G snv 0.51 1