Variant (rsID / SNP)

rs2415129

rs2415129 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO9A. Location: chromosome 15, position 72,191,266. The table records no clinical significance for this variant.

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Reference-table entries

MYO9ANot classified

Variant type: missense_variant
Chromosome / position: 15:72191266
HGVS: NM_006901.4,c.3578G>A,p.Gly1193Glu
Allele change: Missense_G1193E

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.