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: rs41268753
rs41268753
3 0.882 0.200 1 24342967 missense variant C/T snv 2.3E-02 2.3E-02 0.030 0.667 3 2016 2018
dbSNP: rs2486668
rs2486668
6 0.807 0.320 1 24331573 missense variant C/G snv 0.16 0.17 0.010 < 0.001 1 2016 2016
dbSNP: rs545809
rs545809
3 0.882 0.200 1 24364274 missense variant T/A snv 0.29 0.26 0.010 < 0.001 1 2016 2016