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: rs1035550
rs1035550
1 1.000 0.040 16 86569101 3 prime UTR variant A/C;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs34221221
rs34221221
1 1.000 0.040 16 86566824 intron variant C/G;T snv 0.010 1.000 1 2016 2016