RS121907987 PHGDH

Health Risk Chr 1:119743905 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
PHGDH deficiency
See cases
Neu-Laxova syndrome 1
PHGDH-related disorder
PHGDH deficiency
See cases
Neu-Laxova syndrome 1
PHGDH-related disorder
Population Frequencies
gnomAD ALL
0%
Other Variants in PHGDH
rs121907988 rs730882181 rs267606949 rs267606948 rs267606947 rs587777770 rs587777483 rs587777774 rs886041874 rs148078511
Ask Dr. Hemsworth about this variant