Variant (rsID / SNP)

rs11082795

rs11082795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO5B. Location: chromosome 18, position 47,500,836. Clinical significance in the table: Benign.

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Reference-table entries

MYO5BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:47500836
Cytoband: 18q21.1
HGVS: NM_001080467.3(MYO5B):c.1206C>T (p.Asn402=)
Allele change: Synonymous_N402N

Associated conditions / phenotypes

Congenital microvillous atrophy

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.