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: rs11221332
rs11221332
13 0.763 0.280 11 128511079 intron variant C/A;T snv 0.800 1.000 1 2010 2010
dbSNP: rs61907765
rs61907765
1 1.000 0.080 11 128522042 5 prime UTR variant C/G;T snv 0.17 0.15 0.800 1.000 1 2011 2011
dbSNP: rs4128561
rs4128561
1 1.000 0.080 11 128545234 intron variant T/C snv 0.58 0.700 1.000 1 2016 2016