RS121913582 MTR

Health Risk Chr 1:236835586
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Methylcobalamin deficiency type cblG
Neural tube defects
folate-sensitive
Methylcobalamin deficiency type cblG
Neural tube defects
folate-sensitive
Other Variants in MTR
rs121913578 rs121913579 rs1661117141 rs797044444 rs797044445 rs121913580 rs121913581 rs794727395 rs116836001 rs142857114
Ask Dr. Hemsworth about this variant