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Variant (rsID / SNP)

rs11558990

OLA1

rs11558990 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OLA1. Location: chromosome 2, position 174,946,760. The table records no clinical significance for this variant.

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Reference-table entries

OLA1Not classified
Variant type
missense_variant
Chromosome / position
2:174946760
HGVS
NM_013341.5,c.761A>G,p.Tyr254Cys
Allele change
Missense_Y254C

Public references

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