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: rs35390
rs35390
1 1.000 0.040 5 33955221 intron variant C/A snv 0.81 0.800 1.000 1 2011 2011
dbSNP: rs16891982
rs16891982
13 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.750 0.833 6 2008 2017
dbSNP: rs35407
rs35407
6 0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs35414
rs35414
1 1.000 0.040 5 33969523 intron variant T/C snv 0.45 0.010 1.000 1 2011 2011