Variant (rsID / SNP)

rs2431352

rs2431352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQGAP2. Location: chromosome 5, position 75,923,294. The table records no clinical significance for this variant.

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Reference-table entries

IQGAP2Not classified

Variant type: missense_variant
Chromosome / position: 5:75923294
HGVS: NM_006633.5,c.1581T>G,p.Asp527Glu
Allele change: Missense_D527E

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.