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: rs557277320
rs557277320
1 15 65757263 intron variant GGG/-;G;GG;GGGG;GGGGG;GGGGGG delins 0.700 1.000 1 2016 2016
dbSNP: rs6494537
rs6494537
2 15 65759007 intron variant C/G;T snv 0.700 1.000 1 2010 2010