Variant (rsID / SNP)

rs114788132

rs114788132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNA2. Location: chromosome 10, position 70,225,520. Clinical significance in the table: Benign.

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Reference-table entries

DNA2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:70225520
Cytoband: 10q21.3
HGVS: NM_001080449.3(DNA2):c.491A>G (p.Glu164Gly)
Allele change: Missense_E164G

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.