Source: ALL
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: rs1884613
rs1884613
LOC105372629
7 0.807 0.200 20 44351775 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018