Variant (rsID / SNP)

rs2290305

rs2290305 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARPC4-TTLL3, TTLL3. Location: chromosome 3, position 9,871,030. The table records no clinical significance for this variant.

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Reference-table entries

ARPC4-TTLL3Not classified

Variant type: missense_variant
Chromosome / position: 3:9871030
HGVS: NM_001198793.1,c.1688T>G,p.Met563Arg
Allele change: Missense_M563R

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.