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: rs4963128
rs4963128
3 0.882 0.120 11 589564 intron variant T/C snv 0.64 0.830 1.000 5 2008 2012
dbSNP: rs702966
rs702966
2 0.925 0.080 11 611919 3 prime UTR variant C/G snv 0.33 0.020 1.000 2 2010 2011