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: rs121964852
rs121964852
TPM3
4 0.851 0.080 1 154172971 missense variant C/T snv 0.700 0
dbSNP: rs121964854
rs121964854
TPM3
3 0.882 0.080 1 154172972 missense variant G/A;C snv 0.700 0