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: rs727505372
rs727505372
3 0.925 0.040 12 57013359 missense variant G/T snv 0.700 0
dbSNP: rs1396024828
rs1396024828
1 1.000 0.040 12 57013615 synonymous variant C/A snv 0.010 1.000 1 2012 2012
dbSNP: rs1406099149
rs1406099149
1 1.000 0.040 12 57013617 synonymous variant G/A snv 0.010 1.000 1 2012 2012