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: rs104893882
rs104893882
WFS1
1 1.000 0.120 4 6301696 missense variant A/C;G snv 8.0E-06 0.800 1.000 9 2001 2014
dbSNP: rs104893883
rs104893883
WFS1
1 1.000 0.120 4 6302281 missense variant T/C snv 0.800 1.000 9 2001 2014
dbSNP: rs28937893
rs28937893
WFS1
2 0.925 0.120 4 6301941 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.800 0
dbSNP: rs121912618
rs121912618
WFS1
1 1.000 0.120 4 6302371 missense variant G/A;T snv 2.0E-05 0.700 1.000 9 2001 2014
dbSNP: rs141328044
rs141328044
WFS1
1 1.000 0.120 4 6302130 missense variant G/A;T snv 1.7E-03; 4.0E-06 0.700 1.000 9 2001 2014
dbSNP: rs142668478
rs142668478
WFS1
2 0.925 0.120 4 6301849 missense variant G/A;C;T snv 1.8E-04; 4.0E-06 0.700 1.000 9 2001 2014
dbSNP: rs201064551
rs201064551
WFS1
1 1.000 0.120 4 6301752 missense variant C/G;T snv 7.2E-04 0.700 1.000 9 2001 2014
dbSNP: rs758281375
rs758281375
WFS1
1 1.000 0.120 4 6291247 missense variant G/A;C snv 9.6E-05; 4.0E-06 0.700 1.000 9 2001 2014
dbSNP: rs74315205
rs74315205
WFS1 ; LOC107986257
7 0.807 0.360 4 6302385 missense variant G/A snv 0.700 1.000 1 2011 2011
dbSNP: rs1323852277
rs1323852277
WFS1
2 0.925 0.120 4 6301903 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs28937895
rs28937895
WFS1
1 1.000 0.120 4 6302287 missense variant G/A;C snv 8.1E-06 0.700 0