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: rs1199277582
rs1199277582
MTHFR
1 1.000 0.080 1 11801296 missense variant T/C snv 1.2E-05 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs1351260902
rs1351260902
MPO
1 1.000 0.080 17 58279839 missense variant C/G;T snv 0.010 1.000 1 2008 2008