Variant (rsID / SNP)

rs10219555

rs10219555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MON2. Location: chromosome 12, position 62,928,633. The table records no clinical significance for this variant.

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Reference-table entries

MON2Not classified

Variant type: missense_variant
Chromosome / position: 12:62928633
HGVS: NM_015026.3,c.1642G>A,p.Ala548Thr
Allele change: Missense_A548T

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.