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: rs2780831
rs2780831
1 1.000 0.040 1 64880504 intron variant C/T snv 0.35 0.010 < 0.001 1 2018 2018