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: rs11638352
rs11638352
2 0.925 0.040 15 44000939 intron variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs2733201
rs2733201
2 0.925 0.040 15 44116203 intron variant T/A;C snv 0.700 1.000 1 2017 2017