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: rs10465885
rs10465885
4 0.882 0.080 1 147760632 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs121434557
rs121434557
4 0.882 0.200 1 147758953 missense variant C/A;T snv 1.2E-04 2.0E-04 0.010 1.000 1 2013 2013