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: rs1470530779
rs1470530779
1 1.000 0.120 11 68406769 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs1273567061
rs1273567061
1 1.000 0.120 11 68386525 missense variant A/G snv 4.0E-06 2.1E-05 0.700 0
dbSNP: rs760548029
rs760548029
1 1.000 0.120 11 68357768 missense variant G/A snv 4.0E-06 7.0E-06 0.700 1.000 5 2001 2008
dbSNP: rs1158745675
rs1158745675
1 1.000 0.120 11 68386367 stop gained C/A;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs757888034
rs757888034
1 1.000 0.120 11 68386600 missense variant G/A;T snv 1.2E-05; 4.0E-06 1.4E-05 0.700 0
dbSNP: rs1320065036
rs1320065036
2 0.925 0.160 11 68386342 missense variant C/T snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs750791263
rs750791263
1 1.000 0.120 11 68386510 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs80358313
rs80358313
3 0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05 0.700 1.000 5 2001 2008
dbSNP: rs397514665
rs397514665
1 1.000 0.120 11 68363791 missense variant C/T snv 1.2E-05 0.800 1.000 5 2001 2008
dbSNP: rs149645175
rs149645175
1 1.000 0.120 11 68448822 stop gained C/G;T snv 3.7E-05 0.700 0
dbSNP: rs377258285
rs377258285
1 1.000 0.120 11 68425202 missense variant C/T snv 5.6E-05 6.3E-05 0.700 1.000 5 2001 2008
dbSNP: rs201320326
rs201320326
1 1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04 0.700 1.000 5 2001 2008