Variant (rsID / SNP)

rs1002392

rs1002392 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C12ORF56, C12orf56. Location: chromosome 12, position 64,669,090. The table records no clinical significance for this variant.

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Reference-table entries

C12ORF56Not classified

Variant type: synonymous_variant
Chromosome / position: 12:64669090
HGVS: NM_001170633.2,c.1497G>T,p.Leu499Leu
Allele change: Synonymous_L339L

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.