Variant (rsID / SNP)

rs74129447

rs74129447 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLG. Location: chromosome 1, position 152,275,789. Clinical significance in the table: Likely benign.

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Reference-table entries

FLGLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:152275789
Cytoband: 1q21.3
HGVS: NM_002016.2(FLG):c.11573G>A (p.Arg3858His)
Allele change: Missense_R3858H

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.