Variant (rsID / SNP)

rs483216

rs483216 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VSIG10L2. Location: chromosome 11, position 125,818,237. The table records no clinical significance for this variant.

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Reference-table entries

VSIG10L2Not classified

Variant type: synonymous_variant
Chromosome / position: 11:125818237
HGVS: NM_001365077.2,c.471G>A,p.Pro157Pro

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.