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: rs387865
rs387865
1 1.000 0.080 19 11173863 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs4804149
rs4804149
1 1.000 0.080 19 11173352 intron variant T/C snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs8111456
rs8111456
1 1.000 0.080 19 11190471 intron variant A/C;G snv 0.33 0.700 1.000 1 2013 2013