Variant (rsID / SNP)

rs28722602

rs28722602 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSF2RA. Clinical significance in the table: Benign.

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Reference-table entries

CSF2RABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp22.33;Yp11.2
HGVS: NM_172245.4(CSF2RA):c.*49G>T
Allele change: Missense_R358L

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.