Variant (rsID / SNP)

rs61738888

rs61738888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLASP2. Location: chromosome 3, position 33,728,610. The table records no clinical significance for this variant.

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Reference-table entries

CLASP2Not classified

Variant type: missense_variant
Chromosome / position: 3:33728610
HGVS: NM_001365628.1,c.488T>C,p.Leu163Pro
Allele change: Missense_L163P

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.