Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27