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: rs35914442
rs35914442
2 8 60724328 intron variant A/G snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs4449834
rs4449834
2 8 60843309 intron variant G/T snv 0.71 0.700 1.000 1 2016 2016
dbSNP: rs7846314
rs7846314
5 8 60738272 intron variant A/T snv 0.27 0.700 1.000 1 2016 2016