Variant (rsID / SNP)

rs35737219

rs35737219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTHFR. Location: chromosome 1, position 11,850,750. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MTHFRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:11850750
Cytoband: 1p36.22
HGVS: NM_005957.5(MTHFR):c.1958C>T (p.Thr653Met)
Allele change: Missense_T653M

Associated conditions / phenotypes

Homocystinuria due to methylene tetrahydrofolate reductase deficiency|Homocystinuria due to MTHFR deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.