Variant (rsID / SNP)

rs7386782

rs7386782 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OC90. Location: chromosome 8, position 133,053,309. The table records no clinical significance for this variant.

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Reference-table entries

OC90Not classified

Variant type: missense_variant
Chromosome / position: 8:133053309
HGVS: NM_001080399.3,c.439A>G,p.Ser147Gly
Allele change: Missense_S147G

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.