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: rs1623003
rs1623003
1 1.000 0.040 18 23585199 intron variant C/T snv 0.74 0.700 1.000 1 2018 2018