Variant (rsID / SNP)

rs3746736

rs3746736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSTL1. Location: chromosome 20, position 23,424,613. The table records no clinical significance for this variant.

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Reference-table entries

CSTL1Not classified

Variant type: missense_variant
Chromosome / position: 20:23424613
HGVS: NM_138283.1,c.262T>C,p.Trp88Arg
Allele change: Missense_W88R

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.