Variant (rsID / SNP)

rs4875053

rs4875053 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQANK1. Location: chromosome 8, position 144,872,411. The table records no clinical significance for this variant.

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Reference-table entries

IQANK1Not classified

Variant type: missense_variant
Chromosome / position: 8:144872411
HGVS: NM_001381874.1,c.1394C>G,p.Thr465Arg

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.