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: rs28954113
rs28954113
LEP
1 1.000 0.080 7 128254568 missense variant C/A;T snv 2.0E-05; 1.8E-03 0.030 1.000 3 2010 2016
dbSNP: rs199647957
rs199647957
LEP
1 1.000 0.080 7 128254433 synonymous variant C/G;T snv 8.0E-06; 2.8E-05 0.010 1.000 1 2012 2012
dbSNP: rs200343690
rs200343690
LEP
1 1.000 0.080 7 128254653 missense variant G/C snv 4.0E-06 1.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs200487063
rs200487063
LEP
5 0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 0.010 1.000 1 2015 2015
dbSNP: rs34104384
rs34104384
LEP
5 0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03 0.010 1.000 1 2015 2015
dbSNP: rs724159998
rs724159998
LEP
3 0.882 0.080 7 128254557 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs760165439
rs760165439
LEP
1 1.000 0.080 7 128252062 missense variant A/G snv 8.0E-06 0.010 1.000 1 2018 2018