Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs59901009
SBF2
11 10156890 intron variant T/C snv 0.25 2
rs568645819
SBF2
11 10228118 intron variant TTGT/- delins 2
rs10734650
SBF2
0.925 0.080 11 9820944 intron variant C/T snv 0.83 2
rs1372812
SBF2
0.925 0.040 11 10233236 intron variant T/C snv 2.2E-02 2
rs11042561
SBF2
0.925 0.040 11 9941510 intron variant C/A snv 0.20 2
rs66803065
SBF2
11 10004305 intron variant C/A;T snv 0.19 2
rs418635
SBF2 ; SBF2-AS1
0.925 0.040 11 9796458 intron variant T/C snv 6.6E-02 2
rs75248620
LOC101928008 ; SBF2
11 9887580 intron variant G/A snv 5.5E-02 1
rs12361687
LOC101928008 ; SBF2
11 9868505 intron variant G/A snv 0.27 1
rs7945309
LOC101928008 ; SBF2
1.000 0.040 11 9920885 intron variant C/T snv 0.12 1
rs11042543
LOC101928008 ; SBF2
1.000 0.040 11 9918271 intron variant A/G snv 0.20 1
rs7102482
LOC101928008 ; SBF2
1.000 0.040 11 9923277 intron variant C/T snv 0.30 1
rs360124
LOC105369149 ; SBF2 ; SBF2-AS1
11 9780681 non coding transcript exon variant G/C snv 0.88 1
rs17368443
SBF2
11 10275289 intron variant G/C snv 5.3E-02 1
rs4323860
SBF2
11 10138336 intron variant T/C snv 0.50 1
rs11042662
SBF2
11 10193627 intron variant C/T snv 0.27 1
rs55893317
SBF2
11 10159444 intron variant A/G snv 0.25 1
rs2220970
SBF2
11 9836202 intron variant G/A snv 0.80 1
rs10840349
SBF2
11 10054883 intron variant A/G;T snv 1
rs7122422
SBF2
11 10045715 intron variant G/C snv 0.37 1
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 1
rs1470260
SBF2
11 10253573 intron variant T/C snv 0.20 1
rs117518788
SBF2
11 9980672 intron variant C/T snv 2.9E-02 1
rs11042549
SBF2 ; LOC101928008
1.000 0.040 11 9927031 intron variant A/G;T snv 1