Variant (rsID / SNP)

rs35578357

rs35578357 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO18B. Location: chromosome 22, position 26,272,244. The table records no clinical significance for this variant.

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Reference-table entries

MYO18BNot classified

Variant type: missense_variant
Chromosome / position: 22:26272244
HGVS: NM_001318245.2,c.4172C>T,p.Ser1391Phe
Allele change: Missense_S1390F

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.