Variant (rsID / SNP)

rs7703522

rs7703522 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPB41L4A. Location: chromosome 5, position 111,504,479. The table records no clinical significance for this variant.

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Reference-table entries

EPB41L4ANot classified

Variant type: missense_variant
Chromosome / position: 5:111504479
HGVS: NM_001347887.2,c.1889G>A,p.Arg630His
Allele change: Missense_R630H

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.