Variant (rsID / SNP)

rs188590896

rs188590896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ULK4. Location: chromosome 3, position 41,723,090. Clinical significance in the table: Likely benign.

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Reference-table entries

ULK4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:41723090
Cytoband: 3p22.1
HGVS: NM_017886.4(ULK4):c.2887G>A (p.Val963Met)
Allele change: Silent

Associated conditions / phenotypes

Intellectual disability, moderate

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.