Variant (rsID / SNP)

rs117638434

rs117638434 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDIN1. Location: chromosome 15, position 36,989,578. Clinical significance in the table: Benign.

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Reference-table entries

CDIN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:36989578
Cytoband: 15q14
HGVS: NM_001321759.2(CDIN1):c.531C>T (p.Asn177=)
Allele change: Synonymous_N177N

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.