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: rs12430881
rs12430881
1 1.000 0.120 13 28020665 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs35958982
rs35958982
1 1.000 0.120 13 28034336 missense variant C/T snv 1.3E-02 5.0E-02 0.010 1.000 1 2019 2019