Variant (rsID / SNP)

rs11544238

rs11544238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP9. Location: chromosome 12, position 57,870,155. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ARHGAP9Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 12:57870155
Cytoband: 12q13.3
HGVS: NM_032496.4(ARHGAP9):c.1108T>G (p.Ser370Ala)
Allele change: Missense_S370A

Associated conditions / phenotypes

Coronary artery spasm 3, susceptibility to

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.