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: rs4810485
rs4810485
16 0.732 0.480 20 46119308 intron variant T/A;G snv 0.840 1.000 7 2008 2016
dbSNP: rs4239702
rs4239702
1 1.000 0.120 20 46120612 intron variant T/C snv 0.75 0.800 1.000 2 2014 2019
dbSNP: rs1883832
rs1883832
52 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 0.730 0.750 4 2012 2017
dbSNP: rs1535045
rs1535045
12 0.742 0.360 20 46119460 intron variant C/A;G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs772829518
rs772829518
2 0.925 0.200 20 46122699 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008