Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs398098426
ANKS1B
12 99246167 intron variant TT/-;T;TTT delins 0.20 1
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10432782
SOD1
0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs72798544
COX7A2L
0.882 0.120 2 42372465 intron variant T/G snv 1.3E-02 5
rs3809021
PDGFD
0.882 0.080 11 104164894 upstream gene variant T/G snv 0.61 4
rs556621 1.000 6 44626422 intergenic variant T/G snv 0.73 2
rs61921502
MSRB3
1.000 0.080 12 65438688 intron variant T/G snv 0.10 2
rs734194
NGFR ; LOC100288866
1.000 0.080 17 49514247 3 prime UTR variant T/G snv 9.7E-02 2
rs225132 1 8035440 intron variant T/G snv 0.27 1
rs2304556
FMNL2
2 152617280 intron variant T/G snv 0.36 1
rs497177 6 44628316 intergenic variant T/G snv 0.76 1
rs56031230 12 19018473 regulatory region variant T/G snv 3.6E-02 1
rs587777940
EGFR
7 55202667 missense variant T/G snv 7.0E-06 1
rs75188332 8 132863908 upstream gene variant T/G snv 6.6E-02 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs877087
RYR3
0.882 0.080 15 33582074 intron variant T/C;G snv 4