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: rs2073244
rs2073244
1 14 36660669 intron variant A/G snv 0.33 0.010 1.000 1 2016 2016
dbSNP: rs4904210
rs4904210
5 0.851 0.080 14 36666548 missense variant G/C snv 0.36 0.33 0.010 1.000 1 2016 2016