Variant (rsID / SNP)

rs72731540

rs72731540 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCN4. Location: chromosome 8, position 134,233,024. The table records no clinical significance for this variant.

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Reference-table entries

CCN4Not classified

Variant type: missense_variant
Chromosome / position: 8:134233024
HGVS: NM_003882.4,c.550G>A,p.Val184Ile
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.