Variant (rsID / SNP)

rs1410996

rs1410996 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFH. Location: chromosome 1, position 196,696,933. Clinical significance in the table: risk factor.

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Reference-table entries

CFHRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 1:196696933
Cytoband: 1q31.3
HGVS: NM_000186.4(CFH):c.2237-543=
Allele change: Silent

Associated conditions / phenotypes

Age related macular degeneration 4

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.