Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 7
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs28383314 0.925 0.160 6 32619436 regulatory region variant T/C snv 0.61 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 5
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 5
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 4
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 4
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 4
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90 4
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs17752199 0.925 0.040 6 51542050 upstream gene variant A/C;G;T snv 3
rs6478746 0.925 0.040 9 126605119 intron variant G/A snv 0.72 3
rs9853115 0.925 0.040 3 186413811 intergenic variant T/A;G snv 0.51 3