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Variant (rsID / SNP)

rs2277277

TENM4

rs2277277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TENM4. Location: chromosome 11, position 78,372,536. The table records no clinical significance for this variant.

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Reference-table entries

TENM4Not classified
Variant type
synonymous_variant
Chromosome / position
11:78372536
HGVS
NM_001098816.3,c.7509C>T,p.Leu2503Leu
Allele change
Synonymous_L2503L

Associated conditions / phenotypes

Movement Disease|Essential Tremor|Tremor

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.