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: rs1040079
rs1040079
3 0.882 0.040 6 162792995 intron variant A/G snv 0.31 0.020 1.000 2 2006 2012
dbSNP: rs9356058
rs9356058
1 1.000 0.040 6 162730367 intron variant C/A;T snv 0.020 1.000 2 2012 2013
dbSNP: rs1333955
rs1333955
4 0.851 0.080 6 162792422 intron variant T/A;C snv 0.010 1.000 1 2013 2013