Variant (rsID / SNP)

rs1048118

rs1048118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFP. Clinical significance in the table: Benign.

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Reference-table entries

CFPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_001145252.3(CFP):c.1284C>T (p.Asn428=)
Allele change: Synonymous_N428N

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.