Variant (rsID / SNP)

rs141829168

rs141829168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CUL7. Location: chromosome 6, position 43,013,797. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CUL7Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:43013797
Cytoband: 6p21.1
HGVS: NM_014780.5(CUL7):c.2693C>G (p.Ser898Trp)
Allele change: Missense_S898W

Associated conditions / phenotypes

3M syndrome 1

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.