Variant (rsID / SNP)

rs140627086

rs140627086 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTDP1. Location: chromosome 18, position 77,477,873. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CTDP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:77477873
Cytoband: 18q23
HGVS: NM_004715.5(CTDP1):c.2274G>A (p.Pro758=)
Allele change: Synonymous_P758P

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.