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Small Variation
CNV
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Genetic
Non-genetic
All of V1662
ID
Consequence
Gene/Location
Detail
Geno Type
CHD Type
S3502
missense_variant
MTHFR
NM_005957.5:c.677T>C
C
isolated CHD: NA
S3503
missense_variant
MTHFR
NM_005957.5:c.677T>C
T
isolated CHD: NA
