RS104894178 PHYH

Health Risk Chr 10:13283695
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
REFSUM DISEASE
ADULT
1
Retinitis pigmentosa
Phytanic acid storage disease
Inborn genetic diseases
REFSUM DISEASE
ADULT
1
Retinitis pigmentosa
Phytanic acid storage disease
Inborn genetic diseases
Other Variants in PHYH
rs201578674 rs730882058 rs104894179 rs28939672 rs104894173 rs104894174 rs201499815 rs62619919 rs797045100 rs201979258
Ask Dr. Hemsworth about this variant