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Variant (rsID / SNP)

rs2161916

MYO3B

rs2161916 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO3B. Location: chromosome 2, position 171,073,887. The table records no clinical significance for this variant.

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Reference-table entries

MYO3BNot classified
Variant type
synonymous_variant
Chromosome / position
2:171073887
HGVS
NM_138995.5,c.585G>A,p.Pro195Pro
Allele change
Synonymous_P195P

Public references

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