Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1351623
TACR3
4 103666820 intron variant C/T snv 0.36 2
rs1361108
CENPW
6 126446454 intron variant C/T snv 0.44 2
rs16938437
PHF21A
11 46031024 intron variant C/T snv 0.13 2
rs17266097
SATB2
2 199410486 intron variant C/T snv 0.29 2
rs1861072
UNC80
2 209986910 intron variant T/C snv 0.34 2
rs2003476
CRTC1
19 18695858 intron variant T/C 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
rs3115524
SYCE2 ; GCDH
19 12910545 intron variant G/A;C;T snv 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 2
rs35005436
GTF2I ; LOC101926943
1.000 0.080 7 74720592 intron variant C/A;G;T snv 2
rs35436838
RORB
9 74658994 intron variant T/G snv 9.8E-02 2
rs3784710
MAP2K5
15 67780120 intron variant T/C snv 0.30 2
rs4693089
HELQ
4 83452469 intron variant A/G snv 0.60 2
rs4755720
HSD17B12
11 43607199 intron variant C/T snv 0.60 2
rs62023121
CHD2
15 92916223 intron variant C/T snv 0.12 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
rs6899676
SYCP2L
6 10895027 intron variant A/G snv 0.21 2
rs7037266
KDM4C
9 6942940 intron variant C/A snv 0.40 2
rs7553348
FPGT-TNNI3K ; TNNI3K ; LRRC53
1 74539383 intron variant G/A snv 0.42 2
rs7701886
MFAP3
5 154167849 intron variant G/A snv 0.49 2
rs78352137
WDR25
14 100454079 intron variant T/C snv 7.7E-02 2