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: rs10900585
rs10900585
1 1.000 0.040 1 203684896 intron variant G/T snv 0.81 0.810 1.000 2 2012 2013
dbSNP: rs4951074
rs4951074
3 1.000 0.040 1 203691653 intron variant A/G;T snv 0.700 1.000 1 2012 2012