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: rs10415622
rs10415622
1 1.000 19 2739698 intron variant A/G snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs4806874
rs4806874
1 1.000 19 2738354 intron variant A/C;G;T snv 0.010 1.000 1 2010 2010