rs878853006
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs878853006(A;T) |
Make rs878853006(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 4 |
Position | 158680589 |
Gene | ETFDH |
is a | snp |
is | mentioned by |
dbSNP | rs878853006 |
dbSNP (classic) | rs878853006 |
ClinGen | rs878853006 |
ebi | rs878853006 |
HLI | rs878853006 |
Exac | rs878853006 |
Gnomad | rs878853006 |
Varsome | rs878853006 |
LitVar | rs878853006 |
Map | rs878853006 |
PheGenI | rs878853006 |
Biobank | rs878853006 |
1000 genomes | rs878853006 |
hgdp | rs878853006 |
ensembl | rs878853006 |
geneview | rs878853006 |
scholar | rs878853006 |
rs878853006 | |
pharmgkb | rs878853006 |
gwascentral | rs878853006 |
openSNP | rs878853006 |
23andMe | rs878853006 |
SNPshot | rs878853006 |
SNPdbe | rs878853006 |
MSV3d | rs878853006 |
GWAS Ctlg | rs878853006 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853006(T;T) |
Alt | rs878853006(T;T) |
Reference | Rs878853006(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETFDH |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.159601741A>T |
CLNSRC | |
CLNACC | RCV000224742.1, |