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: rs1417182
rs1417182
1 1.000 0.040 6 101885466 intron variant G/A snv 0.40 0.010 1.000 1 2011 2011
dbSNP: rs1556995
rs1556995
1 1.000 0.040 6 101869470 intron variant C/A;T snv 0.010 1.000 1 2011 2011