Variant (rsID / SNP)

rs145499318

rs145499318 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CR2. Location: chromosome 1, position 207,653,397. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CR2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:207653397
Cytoband: 1q32.2
HGVS: NM_001006658.3(CR2):c.3187C>T (p.Arg1063Cys)
Allele change: Missense_R1063C

Associated conditions / phenotypes

Immunodeficiency, common variable, 7

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.