Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05 7
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 7
rs34589476
MET
0.827 0.160 7 116771869 missense variant C/T snv 2.9E-03 3.2E-03 7
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs786202724
MET
0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 5
rs121913668
MET
0.882 0.120 7 116778827 missense variant T/C snv 4
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 4
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs40239
MET
0.851 0.120 7 116677823 intron variant G/A snv 0.87 4
rs121913245
MET
0.925 0.120 7 116783420 missense variant T/C snv 3
rs121913247
MET
0.882 0.200 7 116783359 missense variant T/C snv 3
rs121913670
MET
0.925 0.120 7 116783329 missense variant G/A snv 3
rs121913673
MET
0.925 0.120 7 116782048 missense variant C/G;T snv 3
rs121913676
MET
0.925 0.080 7 116783421 missense variant G/A;C;T snv 3
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs55985569
MET
0.925 0.080 7 116699588 missense variant G/A;T snv 3.7E-03 3
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs765771575
MET
0.882 0.080 7 116782017 missense variant T/C;G snv 4.0E-06; 4.0E-06 3
rs11762213
MET
0.925 0.120 7 116699228 synonymous variant G/A snv 3.3E-02 3.3E-02 2
rs121913244
MET
0.925 0.120 7 116777409 missense variant C/T snv 2
rs121913669
MET
0.925 0.120 7 116782027 missense variant G/A;T snv 4.0E-06 2
rs121913675
MET
0.925 0.080 7 116778953 missense variant C/T snv 2