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: rs11669910
rs11669910
2 19 45238075 intron variant A/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs73036517
rs73036517
4 19 45241584 intron variant A/G snv 0.20 0.700 1.000 1 2016 2016