Variant (rsID / SNP)

rs2242416

rs2242416 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRIP3, SLC22A7. Location: chromosome 6, position 43,273,604. The table records no clinical significance for this variant.

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Reference-table entries

CRIP3Not classified

Variant type: missense_variant
Chromosome / position: 6:43273604
HGVS: NM_206922.3,c.563T>C,p.Ile188Thr
Allele change: Missense_I188T

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.