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Variant (rsID / SNP)

rs2294996

TCFL5

rs2294996 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCFL5. Location: chromosome 20, position 61,488,785. The table records no clinical significance for this variant.

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Reference-table entries

TCFL5Not classified
Variant type
synonymous_variant
Chromosome / position
20:61488785
HGVS
NM_006602.4,c.1200A>G,p.Gln400Gln
Allele change
Synonymous_Q400Q

Public references

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