Variant (rsID / SNP)

rs12207746

rs12207746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EYS. Location: chromosome 6, position 66,042,231. The table records no clinical significance for this variant.

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Reference-table entries

EYSNot classified

Variant type: missense_variant
Chromosome / position: 6:66042231
HGVS: NM_001142801.2,c.1846A>C,p.Ile616Leu
Allele change: Silent

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.