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: rs11959928
rs11959928
C9 ; DAB2
4 1.000 0.080 5 39397030 intron variant T/A snv 0.39 0.700 1.000 2 2010 2016
dbSNP: rs10062079
rs10062079
C9 ; DAB2
1 5 39393631 intron variant G/A snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs700236
rs700236
C9
2 5 39367637 intron variant A/G snv 0.37 0.700 1.000 1 2017 2017