Source: INFERRED ×
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: rs2307449
rs2307449
1 15 89320697 intron variant T/G snv 0.47 0.800 1.000 1 2012 2012
dbSNP: rs1054875
rs1054875
1 15 89335895 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2015 2015