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: rs12220534
rs12220534
1 1.000 0.080 10 43238858 intron variant T/G snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs1879310
rs1879310
1 1.000 0.080 10 43239327 intron variant T/C snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs7090455
rs7090455
1 1.000 0.080 10 43258084 intron variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs7093409
rs7093409
1 1.000 0.080 10 43244619 intron variant A/G snv 0.18 0.700 1.000 1 2009 2009