Variant (rsID / SNP)

rs3744647

rs3744647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF15. Location: chromosome 17, position 8,224,276. The table records no clinical significance for this variant.

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Reference-table entries

ARHGEF15Not classified

Variant type: missense_variant
Chromosome / position: 17:8224276
HGVS: NM_025014.2,c.2491T>C,p.Ser831Pro
Allele change: Missense_S831P

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.