Source: ALL
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: rs1057519090
rs1057519090
COL4A2
7 0.851 0.160 13 110492105 missense variant G/A snv 0.700 0
dbSNP: rs121913528
rs121913528
KRAS
12 0.851 0.160 12 25227349 missense variant C/A;T snv 0.700 0