RS137853061 MTRR

Health Risk Chr 5:7892815
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What This Variant Does
"[OMIM:?]
Associated Conditions
Methylcobalamin deficiency type cblE
Inborn genetic diseases
Neural tube defects
folate-sensitive
Methylcobalamin deficiency type cblE
Inborn genetic diseases
Neural tube defects
folate-sensitive
Other Variants in MTRR
rs2126812944 rs2126808021 rs137853062 rs796052001 rs148909799 rs147277149 rs368391537 rs202110383 rs753947379 rs577851734
Ask Dr. Hemsworth about this variant