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Variant (rsID / SNP)

rs77873910

CCKBR

rs77873910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCKBR. Location: chromosome 11, position 6,291,466. The table records no clinical significance for this variant.

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Reference-table entries

CCKBRNot classified
Variant type
synonymous_variant
Chromosome / position
11:6291466
HGVS
NM_001363552.2,c.552A>G,p.Leu184Leu
Allele change
Synonymous_L100L

Public references

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