Variant (rsID / SNP)

rs2071856

rs2071856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ELFN2. Location: chromosome 22, position 37,770,630. The table records no clinical significance for this variant.

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Reference-table entries

ELFN2Not classified

Variant type: synonymous_variant
Chromosome / position: 22:37770630
HGVS: NM_052906.5,c.945C>T,p.Ile315Ile
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.