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: rs1928168
rs1928168
1 6 22017509 intron variant T/C snv 0.36 0.700 1.000 2 2011 2012
dbSNP: rs2078543
rs2078543
1 6 21996631 intron variant A/G snv 0.69 0.700 1.000 1 2012 2012