Variant (rsID / SNP)

rs564260248

rs564260248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TECPR2. Location: chromosome 14, position 102,894,569. Clinical significance in the table: Likely benign.

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Reference-table entries

TECPR2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:102894569
Cytoband: 14q32.31
HGVS: NM_014844.5(TECPR2):c.952-18T>G
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.