RS1047808762 GRIN2D

Health Risk Chr 19:48443186
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in GRIN2D
rs886040861 rs1569065861 rs1569065866 rs1569064110 rs1303988486 rs149544539 rs1600982197 rs1600982189 rs1970945661 rs1970995171
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