RS757966746 AHCY

Health Risk Chr 20:34294083
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
Inborn genetic diseases
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
Other Variants in AHCY
rs121918607 rs121918608 rs57344541 rs11552695 rs774846394 rs146829385 rs370059571 rs375253690 rs768480898 rs200332864
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