Variant (rsID / SNP)

rs2297879

rs2297879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF39. Location: chromosome 9, position 35,662,251. The table records no clinical significance for this variant.

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Reference-table entries

ARHGEF39Not classified

Variant type: missense_variant
Chromosome / position: 9:35662251
HGVS: NM_032818.3,c.917A>G,p.His306Arg
Allele change: Missense_H306R

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.