Variant (rsID / SNP)

rs7535533

rs7535533 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RGSL1. Location: chromosome 1, position 182,496,829. The table records no clinical significance for this variant.

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Reference-table entries

RGSL1Not classified

Variant type: missense_variant
Chromosome / position: 1:182496829
HGVS: NM_001366934.1,c.2152A>G,p.Ile718Val
Allele change: Missense_I683V

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.