Variant (rsID / SNP)

rs2240234

rs2240234 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFR2. Location: chromosome 19, position 3,831,709. The table records no clinical significance for this variant.

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Reference-table entries

ZFR2Not classified

Variant type: missense_variant
Chromosome / position: 19:3831709
HGVS: NM_015174.2,c.547G>A,p.Val183Met
Allele change: Silent

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.