Variant (rsID / SNP)

rs2051561

rs2051561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE28. Location: chromosome 4, position 2,275,835. The table records no clinical significance for this variant.

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Reference-table entries

ZFYVE28Not classified

Variant type: synonymous_variant
Chromosome / position: 4:2275835
HGVS: NM_020972.3,c.2160C>T,p.Phe720Phe
Allele change: Synonymous_F720F

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.