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: rs7825271
rs7825271
2 8 68651460 intron variant G/T snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs920016
rs920016
1 8 68628983 intron variant A/C snv 0.14 0.700 1.000 1 2012 2012