Variant (rsID / SNP)

rs146365382

rs146365382 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARS2. Location: chromosome 2, position 198,571,223. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MARS2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:198571223
Cytoband: 2q33.1
HGVS: NM_138395.4(MARS2):c.1094A>G (p.Tyr365Cys)
Allele change: Missense_Y365C

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.