All of V0737

ID Consequence Gene/Location Detail Geno Type CHD Type
S1692 missense_variant NOS3 NM_000603.5:c.894T>G G/G NA: NA
S1693 missense_variant NOS3 NM_000603.5:c.894T>G T/G NA: NA
S1694 missense_variant NOS3 NM_000603.5:c.894T>G T/T NA: NA

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