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Variant (rsID / SNP)

rs5761170

MYO18B

rs5761170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO18B. Location: chromosome 22, position 26,173,661. The table records no clinical significance for this variant.

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Reference-table entries

MYO18BNot classified
Variant type
missense_variant
Chromosome / position
22:26173661
HGVS
NM_001318245.2,c.1981T>C,p.Trp661Arg
Allele change
Missense_W661R

Public references

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