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: rs1109748
rs1109748
2 11 61955173 synonymous variant C/A snv 0.21 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1800009
rs1800009
1 11 61962762 synonymous variant T/C snv 0.46 0.43 0.700 1.000 1 2011 2011