Variant (rsID / SNP)

rs6765537

rs6765537 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C3ORF20, C3orf20. Location: chromosome 3, position 14,755,572. The table records no clinical significance for this variant.

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Reference-table entries

C3ORF20Not classified

Variant type: missense_variant
Chromosome / position: 3:14755572
HGVS: NM_032137.5,c.1219A>G,p.Ile407Val
Allele change: Missense_I285V

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.