Variant (rsID / SNP)

rs3219201

rs3219201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAPK8IP2. Location: chromosome 22, position 51,043,278. The table records no clinical significance for this variant.

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Reference-table entries

MAPK8IP2Not classified

Variant type: synonymous_variant
Chromosome / position: 22:51043278
HGVS: NM_012324.6,c.1548G>A,p.Glu516Glu
Allele change: Missense_S517N

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.