EgPeds: Example pedigrees
In simrvprojects/SimRVPedigree: Simulate Pedigrees Ascertained for a Rare Disease

A dataset containing five example pedigrees.

1	data(EgPeds)

A data frame with 65 rows and 14 variables:

FamID: Family identification number
ID: Individual identification number
sex: Gender identification variable: sex = 0 for males, and sex = 1 females.
dadID: Identification number of father
momID: Identification number of mother
affected: Affection status: affected = TRUE if individual has developed lymphoid cancer, and FALSE otherwise.
DA1: Paternally inherited allele at the assumed disease locus: DA1 = 1 if rare variant is present, and 0 otherwise.
DA2: Maternally inherited allele at the assumed disease locus: DA2 = 1 if rare variant is present, and 0 otherwise.
birthYr: Year of birth
onsetYr: Year of disease onset, when applicable.
deathYr: Year of death, when applicable.
RR: The subject's relative-risk of disease
available: Availability status, available = TRUE if the individual is unavailable, and FALSE 1 otherwise
Gen: The subject's generation number relative to the founder who introduced the rare variant. That is, the founder who introduced the rare variant will have Gen = 1, his or her offspring will have Gen = 2, etc.
proband: Proband identification variable, proband = TRUE if the individual is the proband, and FALSE otherwise.