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: rs999737
rs999737
8 0.776 0.200 14 68567965 intron variant C/T snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs11158728
rs11158728
1 1.000 0.120 14 68295488 intron variant G/A;C;T snv 0.010 1.000 1 2011 2011
dbSNP: rs927220
rs927220
1 1.000 0.120 14 68301255 intron variant G/T snv 0.69 0.010 1.000 1 2011 2011