Variant (rsID / SNP)

rs2293624

rs2293624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C12ORF73, C12orf73. Location: chromosome 12, position 104,345,384. The table records no clinical significance for this variant.

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Reference-table entries

C12ORF73Not classified

Variant type: missense_variant
Chromosome / position: 12:104345384
HGVS: NM_001135570.3,c.133C>T,p.Arg45Cys
Allele change: Missense_R45C

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.