Variant (rsID / SNP)

rs7093643

rs7093643 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C10ORF62, C10orf62, HOGA1. Location: chromosome 10, position 99,350,128. The table records no clinical significance for this variant.

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Reference-table entries

C10ORF62Not classified

Variant type: synonymous_variant
Chromosome / position: 10:99350128
HGVS: NM_001009997.3,c.474A>G,p.Leu158Leu
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.