Variant (rsID / SNP)

rs55714450

rs55714450 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2ORF73, C2orf73. Location: chromosome 2, position 54,562,012. The table records no clinical significance for this variant.

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Reference-table entries

C2ORF73Not classified

Variant type: missense_variant
Chromosome / position: 2:54562012
HGVS: NM_001100396.2,c.85C>A,p.His29Asn
Allele change: Missense_H29N

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.