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: rs10419408
rs10419408
2 19 12831936 intron variant A/G snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs4804737
rs4804737
2 19 12837124 intron variant T/C snv 0.40 0.700 1.000 1 2009 2009