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Variant (rsID / SNP)

rs7542665

L1TD1

rs7542665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to L1TD1. Location: chromosome 1, position 62,673,037. The table records no clinical significance for this variant.

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Reference-table entries

L1TD1Not classified
Variant type
missense_variant
Chromosome / position
1:62673037
HGVS
NM_001164835.2,c.737T>C,p.Val246Ala
Allele change
Missense_V246A

Public references

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