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.glm.firth

Same column layout as .glm.logistic when Firth logistic regression is used (extension .glm.firth or .glm.logistic.hybrid).

Overview

Field Value
Format key plink2_firth
Spec file formats/plink2_firth.json
Cite name PLINK 2.0
Version PLINK 2.0 (doc revision 11 Mar 2026)
Last checked 20260326
Source https://www.cog-genomics.org/plink/2.0/formats#glm_logistic
Citation Chang, C. C., Chow, C. C., Tellier, L. C., Vattikuti, S., Purcell, S. M., & Lee, J. J. (2015). Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience, 4(1), s13742-015.
## File layout
Field Value
Separator TAB
NA value .
Comment prefix #
Header row yes
Column order #CHROM, POS, ID, REF, ALT1, ALT, PROVISIONAL_REF?, A1, OMITTED, A1_CT, ALLELE_CT, A1_CASE_CT, A1_CTRL_CT, CASE_ALLELE_CT, CTRL_ALLELE_CT, CASE_NON_A1_CT, CASE_HET_A1_CT, CASE_HOM_A1_CT, CTRL_NON_A1_CT, CTRL_HET_A1_CT, CTRL_HOM_A1_CT, A1_FREQ, A1_CASE_FREQ, A1_CTRL_FREQ, MACH_R2, FIRTH?, TEST, OBS_CT, BETA, OR, LOG(OR)_SE, L95, U95, Z_STAT, F_STAT, P, ERRCODE, LOG10_P
## Column mapping
Raw header Canonical Canonical (secondary)
#CHROM CHR
A1 EA
A1_CASE_CT
A1_CASE_FREQ EAF_CASE
A1_CT
A1_CTRL_CT
A1_CTRL_FREQ EAF_CONTROL
A1_FREQ EAF
ALLELE_CT
ALT ALT
ALT1
BETA BETA
CASE_ALLELE_CT
CASE_HET_A1_CT
CASE_HOM_A1_CT
CASE_NON_A1_CT
CHROM CHR
CTRL_ALLELE_CT
CTRL_HET_A1_CT
CTRL_HOM_A1_CT
CTRL_NON_A1_CT
ERRCODE
F_STAT F
FIRTH?
ID SNPID rsID
L95 OR_95L
LOG(OR)_SE SE
LOG10_P MLOG10P
MACH_R2 INFO
OBS_CT N
OMITTED
OR OR
P P
POS POS
PROVISIONAL_REF?
REF REF
SE SE
TEST
U95 OR_95U
Z_STAT Z
## Header descriptions
Column Description
#CHROM Chromosome code
A1 Counted allele in regression
A1_FREQ A1 allele frequency
ALT All alternate alleles (comma-separated)
BETA Log-odds coefficient for A1
ERRCODE Reason for NA result
FIRTH? Whether Firth regression was used ('firth-fallback' only)
ID Variant ID
LOG(OR)_SE Standard error of log-odds (beta)
OBS_CT Samples in regression
OR Odds ratio for A1
P Asymptotic p-value
POS Base-pair coordinate
REF Reference allele
TEST Test identifier
Z_STAT Wald Z-score
## Coverage

8/9 tier groups satisfied.

Tier Status Matched Missing
Variant ID yes SNPID, rsID
Genomic location yes CHR, POS
Effect / other allele partial EA NEA
Effect size yes BETA, OR, Z HR
Uncertainty yes SE
P-value yes P, MLOG10P
Sample size yes N N_CASE
Allele frequency yes EAF MAF, NEAF
Imputation / QC yes INFO
## See also