Variant (rsID / SNP)

rs7633238

rs7633238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COMMD2. Location: chromosome 3, position 149,459,341. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

COMMD2Not classified

Variant type: synonymous_variant
Chromosome / position: 3:149459341
HGVS: NM_016094.4,c.567T>C,p.Asn189Asn
Allele change: Synonymous_N189N

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.