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: rs3745516
rs3745516
2 0.925 0.080 19 50423485 intron variant A/G snv 0.62 0.800 1.000 3 2010 2015
dbSNP: rs1726773
rs1726773
1 1.000 0.080 19 50424313 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs34944112
rs34944112
1 1.000 0.080 19 50423308 intron variant C/T snv 0.11 0.010 1.000 1 2012 2012