RS121907988 PHGDH

Health Risk Chr 1:119742870
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What This Variant Does
"[OMIM:?]
Associated Conditions
PHGDH deficiency
Neu-Laxova syndrome 1
Neurometabolic disorder due to serine deficiency
PHGDH deficiency
Neu-Laxova syndrome 1
Neurometabolic disorder due to serine deficiency
Other Variants in PHGDH
rs121907987 rs730882181 rs267606949 rs267606948 rs267606947 rs587777770 rs587777483 rs587777774 rs886041874 rs148078511
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