Variant (rsID / SNP)

rs77738677

rs77738677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD96. Location: chromosome 3, position 111,342,600. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CD96Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:111342600
Cytoband: 3q13.2
HGVS: NM_005816.5(CD96):c.1181-1G>A
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.