rs7170637
From SNPedia
Orientation | minus |
Stabilized | plus |
Make rs7170637(A;A) |
Make rs7170637(A;G) |
Make rs7170637(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 22903836 |
Gene | CYFIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs7170637 |
dbSNP (classic) | rs7170637 |
ClinGen | rs7170637 |
ebi | rs7170637 |
HLI | rs7170637 |
Exac | rs7170637 |
Gnomad | rs7170637 |
Varsome | rs7170637 |
LitVar | rs7170637 |
Map | rs7170637 |
PheGenI | rs7170637 |
Biobank | rs7170637 |
1000 genomes | rs7170637 |
hgdp | rs7170637 |
ensembl | rs7170637 |
geneview | rs7170637 |
scholar | rs7170637 |
rs7170637 | |
pharmgkb | rs7170637 |
gwascentral | rs7170637 |
openSNP | rs7170637 |
23andMe | rs7170637 |
SNPshot | rs7170637 |
SNPdbe | rs7170637 |
MSV3d | rs7170637 |
GWAS Ctlg | rs7170637 |
Max Magnitude | 0 |
[PMID 24442360] Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders