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: rs16928809
rs16928809
2 11 2915722 intron variant G/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs1661052
rs1661052
1 11 2921363 non coding transcript exon variant G/A snv 0.89 0.700 1.000 1 2018 2018