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Variant (rsID / SNP)

rs140307393

C2CD3

rs140307393 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2CD3. Location: chromosome 11, position 73,796,878. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

C2CD3Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
11:73796878
Cytoband
11q13.4
HGVS
NM_001286577.2(C2CD3):c.3695A>G (p.Asn1232Ser)
Allele change
Missense_N1232S

Public references

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