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Genetic
Non-genetic
All of V1623
ID
Consequence
Gene/Location
Detail
Geno Type
CHD Type
S3389
missense_variant
RNF41
NM_005785.4:c.206T>A
A
NA: NA
S3390
missense_variant
RNF41
NM_005785.4:c.206T>A
T
NA: NA
