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: rs1264622
rs1264622
3 1.000 0.120 6 30289159 non coding transcript exon variant C/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs577217250
rs577217250
1 6 30308903 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTTTTTTTT delins 0.700 1.000 1 2016 2016