Variant (rsID / SNP)

rs59508481

rs59508481 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF26. Location: chromosome 3, position 153,839,959. The table records no clinical significance for this variant.

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Reference-table entries

ARHGEF26Not classified

Variant type: missense_variant
Chromosome / position: 3:153839959
HGVS: NM_001251962.2,c.178C>T,p.Leu60Phe
Allele change: Missense_L60F

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.