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: rs1561673120
rs1561673120
F13A1
1 1.000 0.080 6 6266566 missense variant C/A snv 0.700 0
dbSNP: rs1173258177
rs1173258177
F13A1
1 1.000 0.080 6 6151855 missense variant A/G snv 0.010 1.000 1 1995 1995
dbSNP: rs369187276
rs369187276
F13A1 ; MIR5683
3 0.882 0.080 6 6167531 missense variant C/G;T snv 4.0E-06; 9.1E-05 0.010 1.000 1 2010 2010
dbSNP: rs375129902
rs375129902
F13A1
3 0.882 0.080 6 6151852 missense variant T/C snv 7.2E-05 5.6E-05 0.010 1.000 1 2010 2010