Variant (rsID / SNP)

rs10936599

rs10936599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYNN. Location: chromosome 3, position 169,492,101. Clinical significance in the table: association.

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Reference-table entries

MYNNAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 3:169492101
Cytoband: 3q26.2
HGVS: NM_018657.5(MYNN):c.18C>T (p.His6=)
Allele change: Silent

Associated conditions / phenotypes

Chronic osteomyelitis

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.