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: rs2820315
rs2820315
5 0.882 0.040 1 201903136 intron variant C/T snv 0.23 0.710 1.000 2 2017 2018
dbSNP: rs34091558
rs34091558
2 1.000 0.040 1 201917642 intron variant A/- delins 0.25 0.010 1.000 1 2018 2018