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: rs2075671
rs2075671
ZAN
2 7 100747483 intron variant G/A;C snv 0.800 1.000 1 2009 2009
dbSNP: rs10953302
rs10953302
ZAN
1 7 100767944 synonymous variant C/T snv 0.23 0.20 0.700 1.000 1 2009 2009