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: rs1925690
rs1925690
7 0.784 0.071 6 87157345 intron variant T/A,C snp 0.92 0.700 1 2012 2012
dbSNP: rs749005
rs749005
7 0.784 0.071 6 6283433 intron variant G/T snp 0.14 0.700 1 2012 2012