Variant (rsID / SNP)

rs10900571

rs10900571 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHA6. Location: chromosome 1, position 204,237,416. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHA6Not classified

Variant type: missense_variant
Chromosome / position: 1:204237416
HGVS: NM_014935.5,c.127G>A,p.Val43Ile
Allele change: Missense_V43I

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.