Variant (rsID / SNP)

rs57859638

rs57859638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQCF1. Location: chromosome 3, position 51,930,850. The table records no clinical significance for this variant.

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Reference-table entries

IQCF1Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 3:51930850
HGVS: NM_152397.3,c.169A>G,p.Lys57Glu
Allele change: Missense_K57E

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.