rs7005606
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7005606(G;G) |
Make rs7005606(G;T) |
Make rs7005606(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 32543983 |
Gene | NRG1 |
is a | snp |
is | mentioned by |
dbSNP | rs7005606 |
dbSNP (classic) | rs7005606 |
ClinGen | rs7005606 |
ebi | rs7005606 |
HLI | rs7005606 |
Exac | rs7005606 |
Gnomad | rs7005606 |
Varsome | rs7005606 |
LitVar | rs7005606 |
Map | rs7005606 |
PheGenI | rs7005606 |
Biobank | rs7005606 |
1000 genomes | rs7005606 |
hgdp | rs7005606 |
ensembl | rs7005606 |
geneview | rs7005606 |
scholar | rs7005606 |
rs7005606 | |
pharmgkb | rs7005606 |
gwascentral | rs7005606 |
openSNP | rs7005606 |
23andMe | rs7005606 |
SNPshot | rs7005606 |
SNPdbe | rs7005606 |
MSV3d | rs7005606 |
GWAS Ctlg | rs7005606 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 26650688] Variation at NRG1 genotype related to modulation of small-world properties of the functional cortical network.