Variant (rsID / SNP)

rs2305764

rs2305764 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO9B. Location: chromosome 19, position 17,313,833. Clinical significance in the table: risk factor.

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Reference-table entries

MYO9BRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 19:17313833
Cytoband: 19p13.11
HGVS: NM_004145.4(MYO9B):c.4879-123G>A
Allele change: Silent

Associated conditions / phenotypes

Celiac disease, susceptibility to, 4

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.