Variant (rsID / SNP)

rs1970911

rs1970911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC88C. Location: chromosome 14, position 91,773,494. Clinical significance in the table: Benign.

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Reference-table entries

CCDC88CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:91773494
Cytoband: 14q32.11
HGVS: NM_001080414.4(CCDC88C):c.3083C>T (p.Ala1028Val)
Allele change: Missense_A1028V

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.