Variant (rsID / SNP)

rs10407035

rs10407035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHG2. Location: chromosome 19, position 39,913,634. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHG2Not classified

Variant type: missense_variant
Chromosome / position: 19:39913634
HGVS: NM_022835.3,c.1940G>A,p.Arg647His
Allele change: Missense_R647H

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.