Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28940578
rs28940578
MEFV
16 0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 0.700 1.000 1 2005 2005
dbSNP: rs104895091
rs104895091
MEFV
2 0.925 0.040 16 3243404 inframe deletion CAT/- delins 0.700 0
dbSNP: rs104895097
rs104895097
MEFV
2 0.925 0.040 16 3243205 missense variant C/T snv 2.0E-04 1.1E-04 0.700 0
dbSNP: rs104895105
rs104895105
MEFV
7 0.851 0.120 16 3247171 missense variant G/A snv 0.700 0
dbSNP: rs104895128
rs104895128
MEFV
3 0.882 0.160 16 3243593 missense variant C/A;T snv 3.7E-05 0.700 0
dbSNP: rs28940579
rs28940579
MEFV
13 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 0.700 0
dbSNP: rs28940580
rs28940580
MEFV
17 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 0.700 0
dbSNP: rs61732874
rs61732874
MEFV
2 0.925 0.040 16 3243257 missense variant C/A;T snv 1.8E-03; 1.2E-05 0.700 0
dbSNP: rs61752717
rs61752717
MEFV
72 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 0.700 0