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: rs1229984
rs1229984
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.080 1.000 8 2009 2019
dbSNP: rs1042026
rs1042026
2 1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs1614972
rs1614972
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.010 1.000 1 2014 2014
dbSNP: rs1789903
rs1789903
1 1.000 0.080 4 99340884 intron variant C/A;G snv 0.010 1.000 1 2014 2014