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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