Variant (rsID / SNP)

rs1133834

rs1133834 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTLL5. Location: chromosome 14, position 76,368,544. Clinical significance in the table: Benign.

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Reference-table entries

TTLL5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:76368544
Cytoband: 14q24.3
HGVS: NM_015072.5(TTLL5):c.3800T>C (p.Phe1267Ser)
Allele change: Missense_F1267S

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.