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: rs1320978
rs1320978
1 1 19621479 intron variant A/G snv 0.64 0.700 1.000 1 2012 2012
dbSNP: rs2745217
rs2745217
1 1 19595253 intron variant C/T snv 0.64 0.700 1.000 1 2012 2012
dbSNP: rs2792043
rs2792043
1 1 19598168 non coding transcript exon variant A/C snv 0.64 0.700 1.000 1 2012 2012