Variant (rsID / SNP)

rs4150001

rs4150001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EXO1. Location: chromosome 1, position 242,048,680. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

EXO1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:242048680
Cytoband: 1q43
HGVS: NM_130398.4(EXO1):c.2276G>A (p.Gly759Glu)
Allele change: Missense_G758E

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.