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Genetic
Non-genetic
All of V1597
ID
Consequence
Gene/Location
Detail
Geno Type
CHD Type
S3337
missense_variant
NFATC1
NM_006162.5:c.2251T>G
T
isolated CHD/non-isolated CHD: NA
S3338
missense_variant
NFATC1
NM_006162.5:c.2251T>G
G
isolated CHD/non-isolated CHD: NA