Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7922612
PLCE1
0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs2274224
PLCE1-AS1 ; PLCE1
0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 6
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs2228059
LOC107984200 ; IL15RA
0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 5
rs4462560
NEIL1 ; MIR631 ; MAN2C1
0.851 0.080 15 75355623 3 prime UTR variant G/C snv 0.64 5
rs621559
CFAP57 ; LOC105378685 ; EBNA1BP2
0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs1050631
SLC39A6
0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 4
rs11473
BSG
0.882 0.080 19 582982 3 prime UTR variant C/A;T snv 4
rs11548103
S100A14
0.882 0.080 1 153615864 splice region variant C/T snv 0.40 0.39 4
rs1200055659
S100A16 ; S100A14
0.851 0.080 1 153614902 missense variant G/A snv 7.0E-06 4
rs12672038
CAV1
0.925 0.080 7 116547052 intron variant G/A snv 7.6E-02 4
rs1595066
ERBB4
0.882 0.080 2 211377000 3 prime UTR variant C/T snv 0.28 4
rs16845990
ERBB4
0.882 0.080 2 211378286 3 prime UTR variant T/A;C snv 4
rs2244438
TRAK2
0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 4
rs2890658
CD274
0.925 0.080 9 5465130 intron variant C/A;T snv 4
rs353163
UBA6-AS1 ; TMPRSS11A
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 4
rs3738894
PRKCE
0.882 0.080 2 46187030 3 prime UTR variant G/A snv 1.1E-02 4
rs6588147
LEPR
0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
rs114673809
MTHFR ; C1orf167
0.882 0.080 1 11787703 3 prime UTR variant G/A snv 5.0E-03 3