rs770665020
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs770665020(A;G) |
Make rs770665020(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 51353271 |
Gene | ETFB |
is a | snp |
is | mentioned by |
dbSNP | rs770665020 |
dbSNP (classic) | rs770665020 |
ClinGen | rs770665020 |
ebi | rs770665020 |
HLI | rs770665020 |
Exac | rs770665020 |
Gnomad | rs770665020 |
Varsome | rs770665020 |
LitVar | rs770665020 |
Map | rs770665020 |
PheGenI | rs770665020 |
Biobank | rs770665020 |
1000 genomes | rs770665020 |
hgdp | rs770665020 |
ensembl | rs770665020 |
geneview | rs770665020 |
scholar | rs770665020 |
rs770665020 | |
pharmgkb | rs770665020 |
gwascentral | rs770665020 |
openSNP | rs770665020 |
23andMe | rs770665020 |
SNPshot | rs770665020 |
SNPdbe | rs770665020 |
MSV3d | rs770665020 |
GWAS Ctlg | rs770665020 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770665020(G;G) rs770665020(T;T) |
Alt | rs770665020(G;G) rs770665020(T;T) |
Reference | Rs770665020(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETFB |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.51856525A>T |
CLNSRC | |
CLNACC | RCV000185881.2, |