Variant (rsID / SNP)

rs2270763

rs2270763 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1ORF53, C1orf53. Location: chromosome 1, position 197,874,949. The table records no clinical significance for this variant.

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Reference-table entries

C1ORF53Not classified

Variant type: synonymous_variant
Chromosome / position: 1:197874949
HGVS: NM_001024594.3,c.288T>C,p.Asp96Asp
Allele change: Synonymous_D96D

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.