All of V0046
| ID |
Consequence |
Gene/Location |
Detail |
Geno Type |
CHD Type |
|
S0087 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
C/C |
isolated CHD: NA |
|
S0088 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
C/T |
isolated CHD: NA |
|
S0089 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
T/T |
isolated CHD: NA |
|
S0090 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
C/C |
isolated CHD: NA |
|
S0091 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
C/T |
isolated CHD: NA |
|
S0092 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
T/T |
isolated CHD: NA |
|
S0093 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
T |
isolated CHD: NA |
|
S0094 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
C/C |
isolated CHD: NA |
|
S0095 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
C/T |
isolated CHD: NA |
|
S0096 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
T/T |
isolated CHD: NA |
|
S0097 |
missense_variant |
MTHFR |
NM_005957.5:c.677T>C |
T |
isolated CHD: NA |
