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: rs7567451
rs7567451
1 1.000 0.040 2 156196868 intron variant G/T snv 0.61 0.700 1.000 1 2018 2018