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: rs1424266770
rs1424266770
10 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 0.030 1.000 3 2010 2014
dbSNP: rs964793521
rs964793521
2 0.925 0.080 4 184638460 5 prime UTR variant C/T snv 1.4E-05 0.010 1.000 1 2001 2001