Databases by @genebe
This is a list of databases submitted by @genebe. You can also view these databases in a browser.
alfa
Aggregated allele frequency from dbGaP and dbSNP
alpha-missense
Title of alpha-missense
bayesdel_noaf
BayesDel noAF
cadd_hg19
CADD is a tool for scoring the deleteriousness
cadd_hg38
CADD is a tool for scoring the deleteriousness
ccrs_hg19
Title of ccrs_hg19
ccrs_hg38
Title of ccrs_hg38
clinvar
A Public Database of Genetic Variants
dann_hg19
DANN: Deep Learning-Based Variant Annotation Database
dann_hg38
DANN: Deep Learning-Based Variant Annotation Database, GRCh38 version
dbsnp
The Single Nucleotide Polymorphism Database
dbsnp_hg19
The Single Nucleotide Polymorphism Database, hg19
gnomad-exomes
GnomAD Exomes - Genome Aggregation Database
gnomad-exomes-depth
Depth of the GnomAD Exomes
gnomad-exomes2
Genome Aggregation Database Exomes 2.1.1, GRCh37,
gnomad-genomes
GnomAD Genomes - Genome Aggregation Database
gnomad-genomes2
Genome Aggregation Database Genomes 2.1.1, GRCh37,
gnomad2-exomes-hg19
GnomAD Exomes hg19, v. 2.1.1 - Genome Aggregation Database
gnomad2-genomes-hg19
GnomAD Genomes hg19, v. 2 - Genome Aggregation Database
gnomad3-genomes-depth
Depth of the GnomAD3 Genomes
phastcons100_hg19
phastCons100
phastcons100_hg38
phastCons100
phylop100_hg19
phylop100
phylop100_hg38
phylop100
revel
REVEL - Rare Exome Variant Ensemble Learner
revel_hg19
REVEL hg19
spliceai
SOTA Splicing Variants impact predictions
topmed
Topmed
varity
Improved pathogenicity prediction for rare human missense variants