Variant (rsID / SNP)

rs924326

rs924326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHG7. Location: chromosome 12, position 93,150,102. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHG7Not classified

Variant type: missense_variant
Chromosome / position: 12:93150102
HGVS: NM_001377329.1,c.1571T>C,p.Met524Thr
Allele change: Missense_M212T

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.