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: rs4607103
rs4607103
4 0.882 0.120 3 64726228 intron variant C/T snv 0.28 0.840 1.000 9 2008 2019
dbSNP: rs6795735
rs6795735
7 0.882 0.120 3 64719689 intron variant C/A;G;T snv 0.800 1.000 2 2012 2018
dbSNP: rs111558778
rs111558778
1 1.000 0.080 3 64763995 intron variant G/A snv 7.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs4611812
rs4611812
1 1.000 0.080 3 64713769 intron variant C/A;T snv 0.53 0.700 1.000 1 2012 2012