Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 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
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 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
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 5
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 4
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4