Variant (rsID / SNP)

rs149017832

rs149017832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANO5. Location: chromosome 11, position 22,281,087. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ANO5Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:22281087
Cytoband: 11p14.3
HGVS: NM_213599.3(ANO5):c.1430T>C (p.Met477Thr)
Allele change: Missense_M476T

Associated conditions / phenotypes

Gnathodiaphyseal dysplasia|Autosomal recessive limb-girdle muscular dystrophy type 2L

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.