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Variant (rsID / SNP)

rs2275477

OSCP1

rs2275477 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OSCP1. Location: chromosome 1, position 36,886,117. The table records no clinical significance for this variant.

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Reference-table entries

OSCP1Not classified
Variant type
missense_variant
Chromosome / position
1:36886117
HGVS
NM_001330493.2,c.949G>A,p.Gly317Arg
Allele change
Missense_G307R

Public references

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