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Variant (rsID / SNP)

rs4853575

MYO1B

rs4853575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1B. Location: chromosome 2, position 192,160,875. The table records no clinical significance for this variant.

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Reference-table entries

MYO1BNot classified
Variant type
synonymous_variant
Chromosome / position
2:192160875
HGVS
NM_001130158.3,c.174C>T,p.Tyr58Tyr
Allele change
Synonymous_Y58Y

Public references

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