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Variant (rsID / SNP)

rs2271160

CEMIP

rs2271160 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEMIP. Location: chromosome 15, position 81,212,521. The table records no clinical significance for this variant.

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Reference-table entries

CEMIPNot classified
Variant type
synonymous_variant
Chromosome / position
15:81212521
HGVS
NM_001293298.2,c.1884T>C,p.Cys628Cys
Allele change
Synonymous_C628C

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.