Variant (rsID / SNP)

rs848642

rs848642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FEZ2. Location: chromosome 2, position 36,782,886. The table records no clinical significance for this variant.

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Reference-table entries

FEZ2Not classified

Variant type: missense_variant
Chromosome / position: 2:36782886
HGVS: NM_001042548.2,c.1066C>T,p.Arg356Cys
Allele change: Missense_R356C

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.