Source: BEFREE

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 15
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 9
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
rs40239
MET
0.851 0.120 7 116677823 intron variant G/A snv 0.87 4
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05 4
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 3
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 3
rs55985569
MET
0.925 0.080 7 116699588 missense variant G/A;T snv 3.7E-03 3
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-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
rs121913247
MET
0.882 0.200 7 116783359 missense variant T/C snv 2
rs11762213
MET
0.925 0.120 7 116699228 synonymous variant G/A snv 3.3E-02 3.3E-02 2
rs1621
MET
0.925 0.160 7 116797552 3 prime UTR variant G/A;C snv 2
rs1395763398
MET
0.925 0.040 7 116795891 missense variant G/A snv 4.0E-06 2
rs763196530
MET
1.000 0.080 7 116699177 synonymous variant A/G;T snv 4.0E-06; 4.0E-06 1
rs38841
MET
1.000 0.040 7 116679872 intron variant A/G snv 0.28 1
rs38845
MET
1.000 0.040 7 116681748 intron variant A/G;T snv 1
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 1
rs38850
MET
1.000 0.080 7 116697595 intron variant G/A snv 0.20 1
rs17138945
MET
1.000 0.040 7 116703812 intron variant T/G snv 7.3E-02 1
rs121913673
MET
0.925 0.120 7 116782048 missense variant C/G;T snv 1
rs10215153
MET
1.000 0.040 7 116759077 intron variant G/A snv 0.32 1