Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2274465
KDM4A
1 43655886 intron variant C/G snv 0.27 2
rs2679894
TGFBRAP1
2 105254322 upstream gene variant A/G snv 0.43 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
rs35775580
LOC105375508 ; KLF14
7 130735979 upstream gene variant A/G snv 2.9E-02 2
rs3743266
RORA ; RORA-AS1
15 60489314 3 prime UTR variant T/C snv 0.31 2
rs3784710
MAP2K5
15 67780120 intron variant T/C snv 0.30 2
rs3893384 1.000 0.040 15 79680713 regulatory region variant C/T snv 0.50 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
rs57149692 16 30130700 regulatory region variant G/C snv 0.46 2
rs58029167
ERMP1
1.000 0.080 9 5850375 intergenic variant A/G;T snv 0.30 2
rs6087709 20 35430145 upstream gene variant C/G snv 0.25 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
rs6499244
NFAT5
1.000 0.040 16 69701368 3 prime UTR variant T/A snv 0.64 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
rs7141210 14 100716133 regulatory region variant T/C snv 0.55 2
rs7161194
MIR541
14 101062668 upstream gene variant A/G;T snv 2