Variant (rsID / SNP)

rs1919128

rs1919128 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2ORF16, C2orf16. Location: chromosome 2, position 27,801,759. The table records no clinical significance for this variant.

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Reference-table entries

C2ORF16Not classified

Variant type: missense_variant
Chromosome / position: 2:27801759
HGVS: NM_032266.5,c.12532A>G,p.Ile4178Val
Allele change: Missense_I774V

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.