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: rs553749201
rs553749201
3 17 4933900 synonymous variant C/A snv 0.700 1.000 1 2016 2016
dbSNP: rs56337033
rs56337033
1 17 4932332 5 prime UTR variant C/T snv 2.5E-03 0.700 1.000 1 2016 2016