Variant (rsID / SNP)

rs36032236

rs36032236 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCC1. Location: chromosome 1, position 109,482,304. The table records no clinical significance for this variant.

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Reference-table entries

CLCC1Not classified

Variant type: missense_variant
Chromosome / position: 1:109482304
HGVS: NM_001048210.3,c.995C>T,p.Ala332Val
Allele change: Missense_A332V

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.