Variant (rsID / SNP)

rs3850315

rs3850315 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARMCX2. The table records no clinical significance for this variant.

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Reference-table entries

ARMCX2Not classified

Variant type: synonymous_variant
HGVS: NM_001282231.2,c.1509G>A,p.Gln503Gln
Allele change: Synonymous_Q503Q

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.