Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 6
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48 5
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs7773004 1.000 0.040 6 26267527 downstream gene variant A/C;G;T snv 4
rs2219939 1.000 0.040 15 78737381 downstream gene variant G/A snv 0.53 3
rs10440708 5 173223484 downstream gene variant A/G snv 4.3E-02 2
rs112827279
LOC102724092
X 15234130 downstream gene variant C/A snv 4.1E-02 2
rs113196862 11 58315137 downstream gene variant C/T snv 4.0E-02 2
rs11864332 16 12883205 downstream gene variant C/T snv 9.2E-02 2
rs140386998 X 100959983 downstream gene variant C/T snv 3.7E-02 2
rs144363312 2 238918088 downstream gene variant T/G snv 6.4E-03 2
rs149502810 11 36265280 downstream gene variant G/A snv 1.9E-02 2
rs1741629 20 23918358 downstream gene variant G/T snv 0.96 2
rs187568415 19 11623811 downstream gene variant G/A snv 4.8E-02 2
rs189478926 11 62196458 downstream gene variant A/G snv 2
rs2160077 14 91962066 downstream gene variant G/A snv 0.44 2
rs55904328 11 76556433 downstream gene variant G/A;C snv 2
rs71417845 14 103210903 downstream gene variant C/G snv 1.7E-02 2
rs74851542 6 41264814 downstream gene variant A/G snv 4.9E-02 2
rs882367 17 61417213 downstream gene variant C/G;T snv 2
rs1383634 15 78737054 downstream gene variant T/C snv 0.53 1
rs4275821 15 78557199 downstream gene variant C/T snv 0.69 1