RS764618040 PHGDH

Health Risk Chr 1:119726868
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What This Variant Does
"CLNSIG=4
Associated Conditions
Epileptic encephalopathy
Seizure
PHGDH deficiency
Inborn genetic diseases
Epileptic encephalopathy
Seizure
PHGDH deficiency
Inborn genetic diseases
Other Variants in PHGDH
rs121907987 rs121907988 rs730882181 rs267606949 rs267606948 rs267606947 rs587777770 rs587777483 rs587777774 rs886041874
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