Variant (rsID / SNP)

rs10456

rs10456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CIB2. Location: chromosome 15, position 78,398,146. Clinical significance in the table: Benign.

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Reference-table entries

CIB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:78398146
Cytoband: 15q25.1
HGVS: NM_006383.4(CIB2):c.477C>T (p.Asp159=)
Allele change: Synonymous_D110D

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.