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: rs3131018
rs3131018
4 1.000 6 31175805 intron variant A/C;G snv 0.800 1.000 1 2010 2010
dbSNP: rs1128175
rs1128175
4 1.000 6 31182658 upstream gene variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs9468877
rs9468877
4 1.000 6 31175126 intron variant G/A snv 0.16 0.700 1.000 1 2010 2010