All of V2387

ID Consequence Gene/Location Detail Geno Type CHD Type
S4710 missense_variant MTHFR NM_005957.5:c.1286A>C A/A NA: NA
S4711 missense_variant MTHFR NM_005957.5:c.1286A>C A/C NA: NA
S4712 missense_variant MTHFR NM_005957.5:c.1286A>C C/C NA: NA
S4713 missense_variant MTHFR NM_005957.5:c.1286A>C A/C+C/C NA: NA