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: rs360721
rs360721
3 0.882 0.200 11 112155193 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs5744292
rs5744292
4 0.851 0.200 11 112143413 3 prime UTR variant T/C snv 0.16 0.010 1.000 1 2011 2011
dbSNP: rs795467
rs795467
2 0.925 0.120 11 112160357 intron variant G/A;C;T snv 0.010 1.000 1 2007 2007