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: rs183511413
rs183511413
2 3 133330418 intron variant A/G snv 2.3E-04 0.700 1.000 1 2017 2017
dbSNP: rs192622883
rs192622883
2 3 133150563 intron variant A/G snv 2.5E-04 0.700 1.000 1 2017 2017