Variant (rsID / SNP)

rs9657362

rs9657362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF10. Location: chromosome 8, position 1,833,801. Clinical significance in the table: Benign.

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Reference-table entries

ARHGEF10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:1833801
Cytoband: 8p23.3
HGVS: NM_014629.4(ARHGEF10):c.1110G>C (p.Leu370Phe)
Allele change: Missense_L332F

Associated conditions / phenotypes

Autosomal dominant slowed nerve conduction velocity|Charcot-Marie-Tooth disease

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.