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Variant (rsID / SNP)

rs4790809

TLCD2

rs4790809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLCD2. Location: chromosome 17, position 1,611,433. The table records no clinical significance for this variant.

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Reference-table entries

TLCD2Not classified
Variant type
synonymous_variant
Chromosome / position
17:1611433
HGVS
NM_001164407.2,c.426T>C,p.Ser142Ser
Allele change
Synonymous_S142S

Public references

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