Variant (rsID / SNP)

rs1560058

rs1560058 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPB41L4A. Location: chromosome 5, position 111,519,740. The table records no clinical significance for this variant.

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Reference-table entries

EPB41L4ANot classified

Variant type: missense_variant
Chromosome / position: 5:111519740
HGVS: NM_001347887.2,c.1595A>G,p.Asn532Ser
Allele change: Missense_N532S

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.