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: rs2528795
rs2528795
1 1.000 0.040 7 74059164 intron variant T/C snv 0.27 0.010 1.000 1 2018 2018