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: rs1913517
rs1913517
2 0.925 0.120 10 48911009 intron variant A/G snv 0.54 0.800 1.000 1 2009 2009
dbSNP: rs2663054
rs2663054
1 1.000 0.080 10 48893932 intron variant A/G snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs7094610
rs7094610
1 1.000 0.080 10 48914136 missense variant C/A snv 0.36 0.28 0.700 1.000 1 2009 2009