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: rs12793832
rs12793832
1 11 67605122 intron variant A/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs1871043
rs1871043
1 11 67607110 non coding transcript exon variant T/C snv 0.39; 4.8E-06 0.45 0.700 1.000 1 2012 2012
dbSNP: rs7948073
rs7948073
1 11 67607713 intron variant T/G snv 0.47 0.700 1.000 1 2012 2012