Variant (rsID / SNP)

rs117099942

rs117099942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO9B. Location: chromosome 19, position 17,311,226. Clinical significance in the table: Benign.

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Reference-table entries

MYO9BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:17311226
Cytoband: 19p13.11
HGVS: NM_004145.4(MYO9B):c.4363G>A (p.Gly1455Ser)
Allele change: Missense_G1455S

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.