rs6711382
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(G;G) | 0 | common in complete genomics |
Make rs6711382(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 151674563 |
Gene | NEB |
is a | snp |
is | mentioned by |
dbSNP | rs6711382 |
dbSNP (classic) | rs6711382 |
ClinGen | rs6711382 |
ebi | rs6711382 |
HLI | rs6711382 |
Exac | rs6711382 |
Gnomad | rs6711382 |
Varsome | rs6711382 |
LitVar | rs6711382 |
Map | rs6711382 |
PheGenI | rs6711382 |
Biobank | rs6711382 |
1000 genomes | rs6711382 |
hgdp | rs6711382 |
ensembl | rs6711382 |
geneview | rs6711382 |
scholar | rs6711382 |
rs6711382 | |
pharmgkb | rs6711382 |
gwascentral | rs6711382 |
openSNP | rs6711382 |
23andMe | rs6711382 |
SNPshot | rs6711382 |
SNPdbe | rs6711382 |
MSV3d | rs6711382 |
GWAS Ctlg | rs6711382 |
GMAF | 0.2599 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs6711382(C;C) Rs6711382(G;G) |
Alt | rs6711382(C;C) Rs6711382(G;G) |
Reference | Rs6711382(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | NEB |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.152531077A>G |
CLNSRC | |
CLNACC | RCV000153548.3, |