Variant (rsID / SNP)

rs3735485

rs3735485 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1G. Location: chromosome 7, position 45,009,341. The table records no clinical significance for this variant.

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Reference-table entries

MYO1GNot classified

Variant type: missense_variant
Chromosome / position: 7:45009341
HGVS: NM_033054.3,c.1466T>C,p.Met489Thr
Allele change: Missense_M489T

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.