Variant (rsID / SNP)

rs1468603

rs1468603 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHG6. Location: chromosome 12, position 6,427,052. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHG6Not classified

Variant type: synonymous_variant
Chromosome / position: 12:6427052
HGVS: NM_001384604.1,c.1095C>T,p.His365His
Allele change: Synonymous_H349H

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.