rs549454407
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs549454407(A;A) |
Make rs549454407(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 158698987 |
Gene | ETFDH |
is a | snp |
is | mentioned by |
dbSNP | rs549454407 |
dbSNP (classic) | rs549454407 |
ClinGen | rs549454407 |
ebi | rs549454407 |
HLI | rs549454407 |
Exac | rs549454407 |
Gnomad | rs549454407 |
Varsome | rs549454407 |
LitVar | rs549454407 |
Map | rs549454407 |
PheGenI | rs549454407 |
Biobank | rs549454407 |
1000 genomes | rs549454407 |
hgdp | rs549454407 |
ensembl | rs549454407 |
geneview | rs549454407 |
scholar | rs549454407 |
rs549454407 | |
pharmgkb | rs549454407 |
gwascentral | rs549454407 |
openSNP | rs549454407 |
23andMe | rs549454407 |
SNPshot | rs549454407 |
SNPdbe | rs549454407 |
MSV3d | rs549454407 |
GWAS Ctlg | rs549454407 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs549454407(A;A) |
Alt | rs549454407(A;A) |
Reference | Rs549454407(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETFDH |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.159620139G>T |
CLNSRC | |
CLNACC | RCV000185896.1, |