Variant (rsID / SNP)

rs2291739

rs2291739 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TIMELESS. Location: chromosome 12, position 56,814,653. The table records no clinical significance for this variant.

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Reference-table entries

TIMELESSNot classified

Variant type: missense_variant
Chromosome / position: 12:56814653
HGVS: NM_003920.5,c.3053C>T,p.Pro1018Leu
Allele change: Silent

Associated conditions / phenotypes

Colorectal Cancer|Mood Disorder|Childhood-Onset Asthma|Asthma

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.