Variant (rsID / SNP)

rs79793560

rs79793560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to REEP4. Location: chromosome 8, position 21,996,453. The table records no clinical significance for this variant.

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Reference-table entries

REEP4Not classified

Variant type: missense_variant
Chromosome / position: 8:21996453
HGVS: NM_025232.4,c.539G>A,p.Arg180Gln
Allele change: Missense_R180Q

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.