Variant (rsID / SNP)

rs2074022

rs2074022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C11ORF21, C11orf21, TSPAN32. Location: chromosome 11, position 2,324,041. The table records no clinical significance for this variant.

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Reference-table entries

C11ORF21Not classified

Variant type: upstream_gene_variant
Chromosome / position: 11:2324041
HGVS: NM_001142946.3,c.-950T>C
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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