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: rs10120653
rs10120653
3 9 134415237 intron variant G/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729
6 9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 0.700 1.000 1 2012 2012
dbSNP: rs34986018
rs34986018
2 9 134433616 intron variant G/A snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs35738419
rs35738419
5 9 134411944 intron variant C/T snv 7.3E-04 0.700 1.000 1 2012 2012