Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs387906592
STAMBPL1 ; ACTA2
0.752 0.280 10 88941309 missense variant C/T snv 14
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs886039303
STAMBPL1 ; ACTA2
0.882 0.160 10 88941310 missense variant G/A snv 5
rs2762939
CYP24A1
0.925 0.160 20 54164712 intron variant G/C;T snv 3
rs28935490
RPL36A-HNRNPH2 ; GLA
1.000 0.160 X 101398432 missense variant C/A;T snv 3.0E-03; 5.4E-06 3
rs1800976
ABCA1 ; LOC105376196
1.000 0.080 9 104928428 intron variant C/G snv 0.47 2
rs2422493
ABCA1 ; LOC105376196
1.000 0.080 9 104928714 intron variant G/A snv 0.48 2