Variant (rsID / SNP)

rs11264498

rs11264498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQGAP3. Location: chromosome 1, position 156,526,387. The table records no clinical significance for this variant.

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Reference-table entries

IQGAP3Not classified

Variant type: missense_variant
Chromosome / position: 1:156526387
HGVS: NM_178229.5,c.1228G>C,p.Val410Leu
Allele change: Missense_V410L

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.