Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs12552
OLFM4
1.000 0.040 13 53051646 3 prime UTR variant A/G snv 0.58 3
rs12602286
EPN2
1.000 0.040 17 19333641 intron variant G/T snv 0.79 3
rs12704290
GRM3-AS1 ; GRM3
1.000 0.040 7 86798310 intron variant G/A snv 8.9E-02 3
rs12826178
SHMT2
1.000 0.040 12 57228588 upstream gene variant G/T snv 5.3E-02 3
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3