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Variant (rsID / SNP)

rs2653601

C11ORF16C11orf16

rs2653601 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C11ORF16, C11orf16. Location: chromosome 11, position 8,942,942. The table records no clinical significance for this variant.

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Reference-table entries

C11ORF16Not classified
Variant type
missense_variant
Chromosome / position
11:8942942
HGVS
NM_020643.3,c.1325G>A,p.Arg442Gln
Allele change
Missense_R442Q

Public references

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