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Variant (rsID / SNP)

rs1800843

CCKBR

rs1800843 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCKBR. Location: chromosome 11, position 6,292,065. The table records no clinical significance for this variant.

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Reference-table entries

CCKBRNot classified
Variant type
synonymous_variant
Chromosome / position
11:6292065
HGVS
NM_001363552.2,c.843C>A,p.Gly281Gly
Allele change
Silent

Associated conditions / phenotypes

Pancreatic Cancer

Public references

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