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: rs2270994
rs2270994
1 11 48136317 intron variant T/C snv 0.58 0.48 0.700 1.000 1 2009 2009
dbSNP: rs7946766
rs7946766
1 11 47982817 intron variant C/A;T snv 0.700 1.000 1 2009 2009