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: rs11066301
rs11066301
12 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs11066320
rs11066320
5 0.925 0.120 12 112468611 intron variant A/G snv 0.70 0.700 1.000 1 2009 2009