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: rs647161
rs647161
10 0.776 0.080 5 135163402 intron variant C/A snv 0.63 0.700 1.000 4 2013 2019
dbSNP: rs254563
rs254563
9 0.790 0.080 5 135104736 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs4976270
rs4976270
10 0.776 0.080 5 135131530 intron variant C/T snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs639933
rs639933
9 0.790 0.080 5 135132061 intron variant C/A snv 0.70 0.700 1.000 1 2019 2019