Variant (rsID / SNP)

rs146405935

rs146405935 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATR. Location: chromosome 3, position 142,281,919. Clinical significance in the table: Benign.

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Reference-table entries

ATRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:142281919
Cytoband: 3q23
HGVS: NM_001184.4(ATR):c.325C>T (p.Arg109Trp)
Allele change: Missense_R109W

Associated conditions / phenotypes

Seckel 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.