##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency">
##FORMAT=<ID=ES,Number=A,Type=Float,Description="Effect size estimate relative to the alternative allele">
##FORMAT=<ID=SE,Number=A,Type=Float,Description="Standard error of effect size estimate">
##FORMAT=<ID=LP,Number=A,Type=Float,Description="-log10 p-value for effect estimate">
##FORMAT=<ID=AF,Number=A,Type=Float,Description="Alternate allele frequency in the association study">
##FORMAT=<ID=SS,Number=A,Type=Integer,Description="Sample size used to estimate genetic effect">
##FORMAT=<ID=EZ,Number=A,Type=Float,Description="Z-score provided if it was used to derive the EFFECT and SE fields">
##FORMAT=<ID=SI,Number=A,Type=Float,Description="Accuracy score of summary data imputation">
##FORMAT=<ID=NC,Number=A,Type=Integer,Description="Number of cases used to estimate genetic effect">
##FORMAT=<ID=ID,Number=1,Type=String,Description="Study variant identifier">
##META=<ID=TotalVariants,Number=1,Type=Integer,Description="Total number of variants in input">
##META=<ID=VariantsNotRead,Number=1,Type=Integer,Description="Number of variants that could not be read">
##META=<ID=HarmonisedVariants,Number=1,Type=Integer,Description="Total number of harmonised variants">
##META=<ID=VariantsNotHarmonised,Number=1,Type=Integer,Description="Total number of variants that could not be harmonised">
##META=<ID=SwitchedAlleles,Number=1,Type=Integer,Description="Total number of variants strand switched">
##META=<ID=TotalControls,Number=1,Type=Integer,Description="Total number of controls in the association study">
##META=<ID=TotalCases,Number=1,Type=Integer,Description="Total number of cases in the association study">
##META=<ID=StudyType,Number=1,Type=String,Description="Type of GWAS study [Continuous or CaseControl]">
##SAMPLE=<ID=finn-b-G6_ALS,TotalVariants=16306907,VariantsNotRead=0,HarmonisedVariants=16277575,VariantsNotHarmonised=29720,SwitchedAlleles=23741,NormalisedVariants=48877,StudyType=Continuous>
##Gwas2VCF_command=--json /mnt/storage/private/mrcieu/research/scratch/IGD/data/dev/finn-b-import/processed/finn-b-G6_ALS/finn-b-G6_ALS_data.json --ref /mnt/storage/private/mrcieu/research/scratch/IGD/data/dev/QC/genomes/b37/human_g1k_v37.fasta; 1.4.0
##file_date=2021-09-04T06:23:43.665331
##bcftools_annotateVersion=1.9-74-g6af271c+htslib-1.9-64-g226b4a8
##bcftools_annotateCommand=annotate -a /mnt/storage/home/gh13047/mr-eve/vcf-reference-datasets/dbsnp/dbsnp.v153.b37.vcf.gz -c ID -o /mnt/storage/private/mrcieu/research/scratch/IGD/data/dev/finn-b-import/processed/finn-b-G6_ALS/finn-b-G6_ALS.vcf.gz -O z /mnt/storage/private/mrcieu/research/scratch/IGD/data/dev/finn-b-import/processed/finn-b-G6_ALS/finn-b-G6_ALS_data.vcf.gz; Date=Sat Sep  4 07:00:37 2021
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	finn-b-G6_ALS
