Variant (rsID / SNP)

rs4956987

rs4956987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHG4B. Location: chromosome 5, position 174,106. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHG4BNot classified

Variant type: missense_variant
Chromosome / position: 5:174106
HGVS: NM_052909.5,c.4295G>A,p.Arg1432Gln
Allele change: Missense_R1432Q

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.