Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 54
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs28940580
MEFV
0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 16
rs224222
MEFV
0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs28940578
MEFV
0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 14
rs28940579
MEFV
0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 10
rs104895105
MEFV
0.851 0.120 16 3247171 missense variant G/A snv 6
rs11466023
MEFV
0.827 0.320 16 3249586 missense variant G/A;T snv 1.5E-02; 4.0E-05 6
rs104895094
MEFV
0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 5
rs104895080
MEFV
0.882 0.160 16 3254380 missense variant C/G;T snv 6.3E-04 2
rs104895081
MEFV
0.925 0.080 16 3254268 missense variant G/A snv 1.6E-04 1.1E-04 2
rs11466024
MEFV
0.925 0.080 16 3249468 missense variant C/A;T snv 1.6E-05; 1.3E-02 2
rs767006697
MEFV
0.925 0.080 16 3254658 frameshift variant C/- delins 2
rs104895076
MEFV
1.000 0.040 16 3254625 missense variant T/A;G snv 7.7E-05; 4.3E-06 1
rs104895083
MEFV
0.925 0.200 16 3247166 missense variant G/C;T snv 4.0E-05; 1.2E-05 1
rs104895097
MEFV
0.925 0.040 16 3243205 missense variant C/T snv 2.0E-04 1.1E-04 1
rs104895128
MEFV
0.882 0.160 16 3243593 missense variant C/A;T snv 3.7E-05 1
rs104895193
MEFV
1.000 0.040 16 3244284 missense variant T/A snv 1
rs1274043842
MEFV
1.000 0.040 16 3248950 missense variant C/T snv 7.0E-06 1
rs190405488
MEFV
1.000 0.040 16 3249609 missense variant C/G snv 2.0E-05 1
rs61732874
MEFV
0.925 0.040 16 3243257 missense variant C/A;T snv 1.8E-03; 1.2E-05 1
rs75977701
MEFV
1.000 0.040 16 3254158 missense variant C/T snv 4.6E-03 3.2E-03 1