Variant (rsID / SNP)

rs35778736

rs35778736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1F. Location: chromosome 19, position 8,618,110. Clinical significance in the table: Benign.

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Reference-table entries

MYO1FBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:8618110
Cytoband: 19p13.2
HGVS: NM_012335.4(MYO1F):c.417C>T (p.His139=)
Allele change: Synonymous_H139H

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.