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: rs11066008
rs11066008
1 1.000 0.080 12 111702865 intron variant A/G snv 9.1E-03 0.700 1.000 1 2011 2011
dbSNP: rs11066015
rs11066015
5 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.700 1.000 1 2011 2011