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: rs2371767
rs2371767
5 3 64732582 intron variant G/C snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs4504165
rs4504165
1 3 64716214 intron variant T/C snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs7638389
rs7638389
1 3 64744216 intron variant G/A snv 0.68 0.700 1.000 1 2017 2017