Variant (rsID / SNP)

rs281385

rs281385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAMSTR. Location: chromosome 19, position 49,217,261. The table records no clinical significance for this variant.

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Reference-table entries

MAMSTRNot classified

Variant type: synonymous_variant
Chromosome / position: 19:49217261
HGVS: NM_001130915.2,c.765T>C,p.Arg255Arg
Allele change: Synonymous_R87R

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.