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: rs189897
rs189897
2 1.000 0.120 3 37477054 intron variant T/A snv 0.13 0.710 1.000 2 2009 2010
dbSNP: rs2212020
rs2212020
1 1.000 0.120 3 37475971 intron variant C/T snv 0.34 0.710 1.000 1 2009 2009
dbSNP: rs169111
rs169111
1 1.000 0.120 3 37474042 intron variant C/T snv 0.84 0.700 1.000 1 2009 2009
dbSNP: rs169188
rs169188
1 1.000 0.120 3 37465958 intron variant G/A snv 7.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs197757
rs197757
1 1.000 0.120 3 37481337 intron variant G/A snv 0.14 0.700 1.000 1 2009 2009