Variant (rsID / SNP)

rs16997517

rs16997517 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSF2RB. Location: chromosome 22, position 37,333,936. Clinical significance in the table: Benign.

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Reference-table entries

CSF2RBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:37333936
Cytoband: 22q12.3
HGVS: NM_000395.3(CSF2RB):c.2086C>T (p.Pro696Ser)
Allele change: Missense_P696S

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.