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: rs1555303073
rs1555303073
6 0.851 0.120 13 110176912 missense variant C/T snv 0.700 0
dbSNP: rs1411040
rs1411040
1 1.000 0.040 13 110291574 intron variant C/T snv 0.84 0.010 1.000 1 2016 2016
dbSNP: rs1961495
rs1961495
1 1.000 0.040 13 110229026 intron variant C/T snv 0.14 0.010 1.000 1 2016 2016