Variant (rsID / SNP)

rs77915386

rs77915386 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1A. Location: chromosome 12, position 57,422,576. Clinical significance in the table: Likely benign.

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Reference-table entries

MYO1ALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:57422576
Cytoband: 12q13.3
HGVS: NM_005379.4(MYO1A):c.3095A>C (p.Lys1032Thr)
Allele change: Missense_K1032T

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.