rs9647635
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9647635(A;A) |
Make rs9647635(A;C) |
Make rs9647635(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 135519918 |
Gene | LINC00271 |
is a | snp |
is | mentioned by |
dbSNP | rs9647635 |
dbSNP (classic) | rs9647635 |
ClinGen | rs9647635 |
ebi | rs9647635 |
HLI | rs9647635 |
Exac | rs9647635 |
Gnomad | rs9647635 |
Varsome | rs9647635 |
LitVar | rs9647635 |
Map | rs9647635 |
PheGenI | rs9647635 |
Biobank | rs9647635 |
1000 genomes | rs9647635 |
hgdp | rs9647635 |
ensembl | rs9647635 |
geneview | rs9647635 |
scholar | rs9647635 |
rs9647635 | |
pharmgkb | rs9647635 |
gwascentral | rs9647635 |
openSNP | rs9647635 |
23andMe | rs9647635 |
SNPshot | rs9647635 |
SNPdbe | rs9647635 |
MSV3d | rs9647635 |
GWAS Ctlg | rs9647635 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
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[PMID 25622261] The influence of AHI1 variants on the diagnosis and treatment outcome in schizophrenia