Variant (rsID / SNP)

rs10109061

rs10109061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LY6H. Location: chromosome 8, position 144,239,859. The table records no clinical significance for this variant.

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Reference-table entries

LY6HNot classified

Variant type: synonymous_variant
Chromosome / position: 8:144239859
HGVS: NM_001130478.2,c.294T>C,p.Cys98Cys
Allele change: Synonymous_C77C

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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