Variant (rsID / SNP)

rs12493885

rs12493885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF26. Location: chromosome 3, position 153,839,866. The table records no clinical significance for this variant.

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Reference-table entries

ARHGEF26Not classified

Variant type: missense_variant
Chromosome / position: 3:153839866
HGVS: NM_001251962.2,c.85G>C,p.Val29Leu
Allele change: Missense_V29L

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.