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: rs1455751791
rs1455751791
3 0.882 0.120 6 152011735 synonymous variant C/G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs2881766
rs2881766
5 0.882 0.120 6 151797984 intron variant T/G snv 0.35 0.010 1.000 1 2019 2019