Variant (rsID / SNP)

rs147531108

rs147531108 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQGAP2. Location: chromosome 5, position 75,886,292. Clinical significance in the table: Benign.

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Reference-table entries

IQGAP2Benign

Clinical significance (as recorded): Benign
Variant type: missense_variant
Chromosome / position: 5:75886292
HGVS: NM_006633.5,c.700G>A,p.Val234Ile
Allele change: Missense_V234I

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.