Variant (rsID / SNP)

rs291102

rs291102 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIGR. Location: chromosome 1, position 207,106,478. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PIGRUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:207106478
Cytoband: 1q32.1
HGVS: NM_002644.4(PIGR):c.1739C>T (p.Ala580Val)
Allele change: Missense_A580V

Associated conditions / phenotypes

IgA glomerulonephritis

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.