rs6468119
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6468119(C;C) |
Make rs6468119(C;T) |
Make rs6468119(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 32544043 |
Gene | NRG1 |
is a | snp |
is | mentioned by |
dbSNP | rs6468119 |
dbSNP (classic) | rs6468119 |
ClinGen | rs6468119 |
ebi | rs6468119 |
HLI | rs6468119 |
Exac | rs6468119 |
Gnomad | rs6468119 |
Varsome | rs6468119 |
LitVar | rs6468119 |
Map | rs6468119 |
PheGenI | rs6468119 |
Biobank | rs6468119 |
1000 genomes | rs6468119 |
hgdp | rs6468119 |
ensembl | rs6468119 |
geneview | rs6468119 |
scholar | rs6468119 |
rs6468119 | |
pharmgkb | rs6468119 |
gwascentral | rs6468119 |
openSNP | rs6468119 |
23andMe | rs6468119 |
SNPshot | rs6468119 |
SNPdbe | rs6468119 |
MSV3d | rs6468119 |
GWAS Ctlg | rs6468119 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26650688] Variation at NRG1 genotype related to modulation of small-world properties of the functional cortical network.