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Variant (rsID / SNP)

rs2271397

LINGO1

rs2271397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINGO1. Location: chromosome 15, position 77,907,775. The table records no clinical significance for this variant.

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Reference-table entries

LINGO1Not classified
Variant type
synonymous_variant
Chromosome / position
15:77907775
HGVS
NM_032808.7,c.474A>G,p.Leu158Leu
Allele change
Synonymous_L152L

Associated conditions / phenotypes

Rapidly Involuting Congenital Hemangioma|Essential Tremor|Tremor|Synonymous_L158L|Synonymous_L152L|Synonymous_L152L|Synonymous_L152L

Public references

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