Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs115777110
LOC107985255
0.882 0.040 1 208936211 intergenic variant T/C snv 1.2E-02 3
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs12128108
AGBL4
0.925 0.040 1 49827749 intron variant C/G;T snv 3
rs12561919
C1orf167 ; C1orf167-AS1
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13 3
rs146330533
ARHGEF10L
0.882 0.040 1 17669971 intron variant G/A snv 1.2E-02 3
rs3027001
CADM3-AS1 ; CADM3
1.000 0.040 1 159199673 intron variant C/G;T snv 3
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs6703335
SDCCAG8
0.882 0.040 1 243445665 intron variant A/G snv 0.50 3
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10489202
MPC2
0.925 0.080 1 167933841 intron variant G/T snv 0.20 2
rs11209970
FOXO6
1.000 0.040 1 41377768 intron variant G/A snv 0.59 2
rs11210195
LOC105378800
1.000 0.040 1 73283600 intergenic variant C/T snv 0.44 2
rs12124523
NEGR1
1.000 0.040 1 72155780 intron variant C/T snv 7.0E-02 2