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: rs2505506
rs2505506
1 1.000 0.080 10 43150406 intron variant C/G;T snv 0.700 1.000 1 2009 2009