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: rs3758349
rs3758349
1 9 133427946 intron variant T/C snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs41314453
rs41314453
2 1.000 0.080 9 133442704 missense variant C/T snv 9.8E-03 9.9E-03 0.700 1.000 1 2018 2018
dbSNP: rs71503194
rs71503194
1 9 133433011 intron variant T/G snv 5.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs72779210
rs72779210
1 9 133434600 intron variant C/T snv 2.5E-02 0.700 1.000 1 2018 2018