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: rs104894023
rs104894023
LEP
1 1.000 7 128254572 missense variant C/T snv 0.800 1.000 2 1998 2015
dbSNP: rs1554394014
rs1554394014
LEP
1 1.000 7 128254720 missense variant T/C snv 0.700 0
dbSNP: rs724159998
rs724159998
LEP
3 0.882 0.080 7 128254557 missense variant G/A;T snv 4.0E-06 0.700 0