Variant (rsID / SNP)

rs162036

rs162036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTRR. Location: chromosome 5, position 7,885,959. Clinical significance in the table: Benign.

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Reference-table entries

MTRRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:7885959
Cytoband: 5p15.31
HGVS: NM_002454.3(MTRR):c.1049A>G (p.Lys350Arg)
Allele change: Missense_K350R

Associated conditions / phenotypes

Gastrointestinal stromal tumor|Disorders of Intracellular Cobalamin Metabolism|Methylcobalamin deficiency type cblE

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.