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: rs11265618
rs11265618
2 1.000 0.080 1 154457616 intron variant C/T snv 0.22 0.010 1.000 1 2018 2018
dbSNP: rs2228145
rs2228145
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2018 2018
dbSNP: rs4329505
rs4329505
3 0.925 0.120 1 154459944 intron variant T/C snv 0.22 0.010 1.000 1 2018 2018