RS121918608 AHCY

Health Risk Chr 20:34292375
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
Inborn genetic diseases
Rhabdomyolysis
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
Inborn genetic diseases
Rhabdomyolysis
Other Variants in AHCY
rs121918607 rs57344541 rs11552695 rs757966746 rs774846394 rs146829385 rs370059571 rs375253690 rs768480898 rs200332864
Ask Dr. Hemsworth about this variant