Variant (rsID / SNP)

rs25689

rs25689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEMIP2. Location: chromosome 9, position 74,360,096. The table records no clinical significance for this variant.

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Reference-table entries

CEMIP2Not classified

Variant type: missense_variant
Chromosome / position: 9:74360096
HGVS: NM_013390.3,c.872G>A,p.Arg291His
Allele change: Silent

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.