Variant (rsID / SNP)

rs41389545

rs41389545 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC45B. Location: chromosome 17, position 33,491,164. 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: 17:33491164
Cytoband: 17q12
HGVS: NM_001267052.2(UNC45B):c.1130A>G (p.Lys377Arg)
Allele change: Missense_K377R

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.