Variant (rsID / SNP)

rs4870887

rs4870887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FER1L6, FER1L6-AS2. Location: chromosome 8, position 125,061,895. The table records no clinical significance for this variant.

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Reference-table entries

FER1L6Not classified

Variant type: synonymous_variant
Chromosome / position: 8:125061895
HGVS: NM_001039112.2,c.2772G>A,p.Lys924Lys
Allele change: Synonymous_K924K

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.