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: rs11575874
rs11575874
1 1.000 0.040 7 155070942 missense variant C/A;T snv 4.3E-02 0.010 1.000 1 2001 2001
dbSNP: rs1800883
rs1800883
1 1.000 0.040 7 155070881 5 prime UTR variant G/C snv 0.42 0.39 0.010 1.000 1 2016 2016