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Small Variation
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Genetic
Non-genetic
All of V1259
ID
Consequence
Gene/Location
Detail
Geno Type
CHD Type
S2646
intron_variant
GART
NM_032195.2:c.77+1138T>C
C
NA: NA
S2647
intron_variant
GART
NM_032195.2:c.77+1138T>C
TT/TC/CC
isolated CHD: SD
