Variant (rsID / SNP)

rs1860967

rs1860967 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to A2ML1. Location: chromosome 12, position 9,013,755. Clinical significance in the table: Benign.

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Reference-table entries

A2ML1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:9013755
Cytoband: 12p13.31
HGVS: NM_144670.6(A2ML1):c.3364C>T (p.Arg1122Trp)
Allele change: Missense_R1122W

Associated conditions / phenotypes

Otitis media, susceptibility to

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.