Variant (rsID / SNP)

rs2277315

rs2277315 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP9. Location: chromosome 12, position 57,869,582. The table records no clinical significance for this variant.

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Reference-table entries

ARHGAP9Not classified

Variant type: missense_variant
Chromosome / position: 12:57869582
HGVS: NM_001319850.2,c.1345A>G,p.Thr449Ala
Allele change: Silent

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.