Gene: COMT ×
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: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.020 1.000 2 2005 2013
dbSNP: rs1445081098
rs1445081098
COMT ; MIR4761
17 0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs769492487
rs769492487
COMT ; MIR4761
2 0.925 0.080 22 19964287 synonymous variant G/A;T snv 8.0E-06; 8.0E-06 0.010 1.000 1 2004 2004