Variant (rsID / SNP)

rs145449046

rs145449046 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFTR. Location: chromosome 7, position 117,232,595. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CFTRUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:117232595
Cytoband: 7q31.2
HGVS: NM_000492.4(CFTR):c.2374C>G (p.Arg792Gly)
Allele change: Missense_R792G

Associated conditions / phenotypes

Cystic fibrosis|Hereditary pancreatitis

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.