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: rs77296290
rs77296290
1 1.000 0.040 6 32667519 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs9274299
rs9274299
2 1.000 0.040 6 32664181 non coding transcript exon variant C/A;G;T snv 1.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs9274390
rs9274390
2 0.925 0.080 6 32664882 missense variant C/G;T snv 3.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs9274623
rs9274623
1 1.000 0.040 6 32668221 intron variant G/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs9274657
rs9274657
2 1.000 0.040 6 32668587 upstream gene variant G/A snv 0.37 0.700 1.000 1 2017 2017