Variant (rsID / SNP)

rs35703638

rs35703638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR36. Location: chromosome 5, position 110,441,839. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

WDR36Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:110441839
Cytoband: 5q22.1
HGVS: NM_139281.3(WDR36):c.1177G>A (p.Ala393Thr)
Allele change: Missense_A449T

Associated conditions / phenotypes

Glaucoma 1, open angle, G|Usher syndrome type 2C

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.