Variant (rsID / SNP)

rs133885

rs133885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO18B. Location: chromosome 22, position 26,159,289. The table records no clinical significance for this variant.

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Reference-table entries

MYO18BNot classified

Variant type: missense_variant
Chromosome / position: 22:26159289
HGVS: NM_001318245.2,c.131G>A,p.Gly44Glu
Allele change: Missense_G44E

Associated conditions / phenotypes

Dyslexia|Dysphasia, Familial Developmental|Dyscalculia|Specific Language Impairment

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.