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: rs11773818
rs11773818
2 0.925 0.080 7 55056275 intron variant C/A;T snv 0.24 0.010 1.000 1 2013 2013
dbSNP: rs17172432
rs17172432
3 0.882 0.080 7 55073624 intron variant T/C snv 0.31 0.010 1.000 1 2013 2013
dbSNP: rs884419
rs884419
2 0.925 0.080 7 55208587 3 prime UTR variant G/A;C snv 0.010 1.000 1 2010 2010