Variant (rsID / SNP)

rs113612355

rs113612355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFI. Location: chromosome 4, position 110,723,140. Clinical significance in the table: Benign.

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Reference-table entries

CFIBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:110723140
Cytoband: 4q25
HGVS: NM_000204.5(CFI):c.-13G>A
Allele change: Silent

Associated conditions / phenotypes

Atypical hemolytic-uremic syndrome with I factor anomaly

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.