rs765556214
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs765556214(A;A) |
Make rs765556214(A;G) |
Make rs765556214(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 11 |
Position | 105933765 |
Gene | GRIA4 |
is a | snp |
is | mentioned by |
dbSNP | rs765556214 |
dbSNP (classic) | rs765556214 |
ClinGen | rs765556214 |
ebi | rs765556214 |
HLI | rs765556214 |
Exac | rs765556214 |
Gnomad | rs765556214 |
Varsome | rs765556214 |
LitVar | rs765556214 |
Map | rs765556214 |
PheGenI | rs765556214 |
Biobank | rs765556214 |
1000 genomes | rs765556214 |
hgdp | rs765556214 |
ensembl | rs765556214 |
geneview | rs765556214 |
scholar | rs765556214 |
rs765556214 | |
pharmgkb | rs765556214 |
gwascentral | rs765556214 |
openSNP | rs765556214 |
23andMe | rs765556214 |
SNPshot | rs765556214 |
SNPdbe | rs765556214 |
MSV3d | rs765556214 |
GWAS Ctlg | rs765556214 |
Max Magnitude | 0 |
aka NM_000829.3(GRIA4):c.2090G>C or (p.Arg697Pro)
OMIM pathogenic variant