Variant (rsID / SNP)

rs10426399

rs10426399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GIPC3. Location: chromosome 19, position 3,589,435. Clinical significance in the table: Benign.

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Reference-table entries

GIPC3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:3589435
Cytoband: 19p13.3
HGVS: NM_133261.3(GIPC3):c.593-6C>T
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.