Gene: MCC ×
Source: CLINVAR ×
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: rs121917731
rs121917731
MCC
1 1.000 0.080 5 113043623 missense variant G/A snv 0.800 0
dbSNP: rs121917732
rs121917732
MCC
1 1.000 0.080 5 113064110 missense variant C/T snv 1.2E-05 0.800 0