rs758218892
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs758218892(C;C) |
Make rs758218892(C;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 158695551 |
Gene | ETFDH |
is a | snp |
is | mentioned by |
dbSNP | rs758218892 |
dbSNP (classic) | rs758218892 |
ClinGen | rs758218892 |
ebi | rs758218892 |
HLI | rs758218892 |
Exac | rs758218892 |
Gnomad | rs758218892 |
Varsome | rs758218892 |
LitVar | rs758218892 |
Map | rs758218892 |
PheGenI | rs758218892 |
Biobank | rs758218892 |
1000 genomes | rs758218892 |
hgdp | rs758218892 |
ensembl | rs758218892 |
geneview | rs758218892 |
scholar | rs758218892 |
rs758218892 | |
pharmgkb | rs758218892 |
gwascentral | rs758218892 |
openSNP | rs758218892 |
23andMe | rs758218892 |
SNPshot | rs758218892 |
SNPdbe | rs758218892 |
MSV3d | rs758218892 |
GWAS Ctlg | rs758218892 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758218892(C;C) |
Alt | rs758218892(C;C) |
Reference | Rs758218892(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETFDH |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.159616703G>C |
CLNSRC | |
CLNACC | RCV000185894.1, |