rs138867882
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs138867882(A;A) |
Make rs138867882(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 47580977 |
Gene | KBTBD4, NDUFS3 |
is a | snp |
is | mentioned by |
dbSNP | rs138867882 |
dbSNP (classic) | rs138867882 |
ClinGen | rs138867882 |
ebi | rs138867882 |
HLI | rs138867882 |
Exac | rs138867882 |
Gnomad | rs138867882 |
Varsome | rs138867882 |
LitVar | rs138867882 |
Map | rs138867882 |
PheGenI | rs138867882 |
Biobank | rs138867882 |
1000 genomes | rs138867882 |
hgdp | rs138867882 |
ensembl | rs138867882 |
geneview | rs138867882 |
scholar | rs138867882 |
rs138867882 | |
pharmgkb | rs138867882 |
gwascentral | rs138867882 |
openSNP | rs138867882 |
23andMe | rs138867882 |
SNPshot | rs138867882 |
SNPdbe | rs138867882 |
MSV3d | rs138867882 |
GWAS Ctlg | rs138867882 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138867882(A;A) |
Alt | rs138867882(A;A) |
Reference | Rs138867882(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFS3 KBTBD4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.47602529G>A |
CLNSRC | |
CLNACC | RCV000479127.1, |