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: rs138094162
rs138094162
1 8 6632047 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs185206099
rs185206099
1 8 6619777 non coding transcript exon variant G/C snv 2.0E-03 0.700 1.000 1 2015 2015
dbSNP: rs186046079
rs186046079
1 8 6611193 intron variant C/T snv 8.2E-04 0.700 1.000 1 2015 2015