Variant (rsID / SNP)

rs7256689

rs7256689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO9B. Location: chromosome 19, position 17,273,893. The table records no clinical significance for this variant.

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Reference-table entries

MYO9BNot classified

Variant type: synonymous_variant
Chromosome / position: 19:17273893
HGVS: NM_004145.4,c.1632G>T,p.Leu544Leu
Allele change: Synonymous_L544L

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.