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: rs441
rs441
4 0.882 0.200 12 111791045 intron variant T/C snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs4646778
rs4646778
1 12 111797979 intron variant C/A snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs671
rs671
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2017 2017
dbSNP: rs886205
rs886205
8 0.827 0.360 12 111766623 intron variant A/G snv 0.35 0.010 1.000 1 2017 2017