RS587777770 PHGDH

Health Risk Chr 1:119727010
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neu-Laxova syndrome 1
PHGDH deficiency
Neu-Laxova syndrome 1
PHGDH deficiency
Other Variants in PHGDH
rs121907987 rs121907988 rs730882181 rs267606949 rs267606948 rs267606947 rs587777483 rs587777774 rs886041874 rs148078511
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