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Variant (rsID / SNP)

rs11235995

C2CD3

rs11235995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2CD3. Location: chromosome 11, position 73,806,443. The table records no clinical significance for this variant.

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Reference-table entries

C2CD3Not classified
Variant type
missense_variant
Chromosome / position
11:73806443
HGVS
NM_001286577.2,c.2990G>A,p.Arg997Gln
Allele change
Missense_R997Q

Public references

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