Variant (rsID / SNP)

rs118204022

rs118204022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR36. Location: chromosome 5, position 110,440,041. Clinical significance in the table: Uncertain significance.

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Reference-table entries

WDR36Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 5:110440041
Cytoband: 5q22.1
HGVS: NM_139281.3(WDR36):c.896A>G (p.Asn299Ser)
Allele change: Missense_N355S

Associated conditions / phenotypes

Glaucoma 1, open angle, G

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.