Variant (rsID / SNP)

rs5951332

rs5951332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARMCX4. The table records no clinical significance for this variant.

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Reference-table entries

ARMCX4Not classified

Variant type: missense_variant
HGVS: NM_001256155.3,c.250A>G,p.Arg84Gly
Allele change: Silent

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.