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: rs1344110
rs1344110
1 1.000 0.040 21 44852737 intron variant T/C snv 0.18 0.010 1.000 1 2017 2017