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: rs9349407
rs9349407
2 1.000 0.080 6 47485642 intron variant G/C snv 0.23 0.830 1.000 4 2011 2015
dbSNP: rs10948363
rs10948363
1 1.000 0.080 6 47520026 intron variant A/G snv 0.23 0.800 1.000 3 2013 2019