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: rs1994016
rs1994016
2 0.851 0.160 15 78787892 intron variant C/T snv 0.30 0.800 1.000 1 2011 2011
dbSNP: rs3825807
rs3825807
2 0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 0.800 1.000 1 2011 2011