Variant (rsID / SNP)

rs115070660

rs115070660 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SF3B4. Location: chromosome 1, position 149,898,292. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SF3B4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:149898292
Cytoband: 1q21.2
HGVS: NM_005850.5(SF3B4):c.682T>C (p.Leu228=)
Allele change: Synonymous_L228L

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.