Variant (rsID / SNP)

rs11654824

rs11654824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC45B. Location: chromosome 17, position 33,513,337. Clinical significance in the table: Benign.

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Reference-table entries

UNC45BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:33513337
Cytoband: 17q12
HGVS: NM_001267052.2(UNC45B):c.2549T>A (p.Ile850Asn)
Allele change: Missense_I850N

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.