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: rs1395621
rs1395621
1 1.000 0.040 1 24944081 intron variant T/C snv 0.64 0.010 1.000 1 2013 2013
dbSNP: rs9438876
rs9438876
2 1.000 0.040 1 24914625 intron variant A/G snv 0.53 0.010 1.000 1 2013 2013