Variant (rsID / SNP)

rs201875016

rs201875016 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GIPC3. Location: chromosome 19, position 3,589,521. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GIPC3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:3589521
Cytoband: 19p13.3
HGVS: NM_133261.3(GIPC3):c.673C>T (p.Arg225Cys)
Allele change: Missense_R225C

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.