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: rs2268797
rs2268797
1 2 31558682 intron variant C/T snv 0.51 0.700 1.000 1 2014 2014
dbSNP: rs2300702
rs2300702
1 2 31562948 intron variant C/A;G;T snv 0.700 1.000 1 2014 2014