Variant (rsID / SNP)

rs1054283

rs1054283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZC2HC1A, IL7. Location: chromosome 8, position 79,610,710. The table records no clinical significance for this variant.

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Reference-table entries

ZC2HC1ANot classified

Variant type: synonymous_variant
Chromosome / position: 8:79610710
HGVS: NM_001362969.2,c.666A>G,p.Leu222Leu
Allele change: Synonymous_L222L

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.