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: rs216158
rs216158
1 1.000 0.040 16 15823981 intron variant C/G snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs9972711
rs9972711
1 1.000 0.040 16 15808733 intron variant A/G;T snv 0.700 1.000 1 2018 2018