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Variant (rsID / SNP)

rs1661714

LLGL2

rs1661714 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LLGL2. Location: chromosome 17, position 73,568,055. The table records no clinical significance for this variant.

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Reference-table entries

LLGL2Not classified
Variant type
synonymous_variant
Chromosome / position
17:73568055
HGVS
NM_001031803.2,c.2370C>T,p.Pro790Pro
Allele change
Synonymous_P790P

Public references

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