Variant (rsID / SNP)

rs2231390

rs2231390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C21ORF62, C21orf62, C21orf62-AS1. Location: chromosome 21, position 34,166,343. The table records no clinical significance for this variant.

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Reference-table entries

C21ORF62Not classified

Variant type: synonymous_variant
Chromosome / position: 21:34166343
HGVS: NM_001162495.3,c.390G>A,p.Glu130Glu
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.