Variant (rsID / SNP)

rs77266350

rs77266350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHA8. Location: chromosome 7, position 30,129,808. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHA8Not classified

Variant type: 3_prime_UTR_variant
Chromosome / position: 7:30129808
HGVS: NM_032639.4,c.*17G>A
Allele change: Silent

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.