Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 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
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs3809627
TBX6 ; YPEL3
16 30091839 5 prime UTR variant C/A snv 0.41 5
rs4449583
TERT
5 1284020 intron variant C/T snv 0.25 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5