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Variant (rsID / SNP)

rs55760516

SPEG

rs55760516 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPEG. Location: chromosome 2, position 220,354,108. The table records no clinical significance for this variant.

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Reference-table entries

SPEGNot classified
Variant type
missense_variant
Chromosome / position
2:220354108
HGVS
NM_005876.5,c.8368A>G,p.Arg2790Gly
Allele change
Missense_R2790G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.