Variant (rsID / SNP)

rs495335

rs495335 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRISP3. Location: chromosome 6, position 49,701,523. The table records no clinical significance for this variant.

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Reference-table entries

CRISP3Not classified

Variant type: missense_variant
Chromosome / position: 6:49701523
HGVS: NM_001368123.1,c.409T>C,p.Ser137Pro
Allele change: Missense_S119P

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.