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: rs141488085
rs141488085
1 1.000 4 103147427 missense variant T/C snv 3.3E-04 3.3E-04 0.800 1.000 1 2014 2014
dbSNP: rs144716013
rs144716013
1 1.000 4 103158691 missense variant C/A;T snv 4.4E-04; 1.3E-04 0.800 1.000 1 2014 2014