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: rs5918
rs5918
26 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 0.020 1.000 2 2004 2014
dbSNP: rs756351287
rs756351287
5 0.827 0.080 12 120325936 missense variant G/A;C;T snv 2.4E-05 0.010 1.000 1 2004 2004