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: rs12075
rs12075
22 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 0.700 1.000 1 2012 2012
dbSNP: rs3027012
rs3027012
3 1 159204333 5 prime UTR variant C/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs863002
rs863002
2 1 159205130 intron variant C/T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs863006
rs863006
2 1 159207958 non coding transcript exon variant G/A snv 0.56 0.700 1.000 1 2012 2012