Variant (rsID / SNP)

rs370520589

rs370520589 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABRAXAS1. Location: chromosome 4, position 84,406,219. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ABRAXAS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:84406219
Cytoband: 4q21.23
HGVS: NM_139076.3(ABRAXAS1):c.7G>C (p.Gly3Arg)
Allele change: Silent

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.