Variant (rsID / SNP)

rs36656

rs36656 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMC4, LENG1. Location: chromosome 19, position 54,664,752. The table records no clinical significance for this variant.

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Reference-table entries

TMC4Not classified

Variant type: synonymous_variant
Chromosome / position: 19:54664752
HGVS: NM_001145303.3,c.1854T>G,p.Leu618Leu
Allele change: Synonymous_L612L

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.