Variant (rsID / SNP)

rs36074676

rs36074676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPVL. Location: chromosome 7, position 29,160,646. The table records no clinical significance for this variant.

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Reference-table entries

CPVLNot classified

Variant type: missense_variant
Chromosome / position: 7:29160646
HGVS: NM_001371264.1,c.32C>T,p.Ser11Leu
Allele change: Missense_S11L

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.