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: rs2871776
rs2871776
1 1 17001806 intron variant T/C snv 0.56 0.010 1.000 1 2012 2012
dbSNP: rs4920608
rs4920608
2 1 16992792 intron variant C/T snv 0.55 0.010 1.000 1 2012 2012