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: rs4239436
rs4239436
3 18 23151966 intron variant A/G snv 0.81 0.700 1.000 1 2017 2017
dbSNP: rs4308051
rs4308051
1 18 23155497 intron variant T/G snv 0.81 0.700 1.000 1 2017 2017
dbSNP: rs4800452
rs4800452
3 18 23147647 intron variant C/G;T snv 0.700 1.000 1 2017 2017