Variant (rsID / SNP)

rs8105710

rs8105710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VSIG10L. Location: chromosome 19, position 51,844,978. The table records no clinical significance for this variant.

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Reference-table entries

VSIG10LNot classified

Variant type: synonymous_variant
Chromosome / position: 19:51844978
HGVS: NM_001163922.3,c.324C>A,p.Ser108Ser
Allele change: Synonymous_S108S

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.