Variant (rsID / SNP)

rs62376783

rs62376783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR36. Location: chromosome 5, position 110,434,448. Clinical significance in the table: Benign.

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Reference-table entries

WDR36Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:110434448
Cytoband: 5q22.1
HGVS: NM_139281.3(WDR36):c.320C>T (p.Ala107Val)
Allele change: Missense_A163V

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.