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: rs12086634
rs12086634
6 0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 0.010 1.000 1 2006 2006
dbSNP: rs846910
rs846910
6 0.882 0.160 1 209701909 intron variant A/G snv 0.95 0.010 1.000 1 2006 2006