rs534517447
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs534517447(A;A) |
Make rs534517447(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 120956935 |
Gene | GRIK4, LOC101929208 |
is a | snp |
is | mentioned by |
dbSNP | rs534517447 |
dbSNP (classic) | rs534517447 |
ClinGen | rs534517447 |
ebi | rs534517447 |
HLI | rs534517447 |
Exac | rs534517447 |
Gnomad | rs534517447 |
Varsome | rs534517447 |
LitVar | rs534517447 |
Map | rs534517447 |
PheGenI | rs534517447 |
Biobank | rs534517447 |
1000 genomes | rs534517447 |
hgdp | rs534517447 |
ensembl | rs534517447 |
geneview | rs534517447 |
scholar | rs534517447 |
rs534517447 | |
pharmgkb | rs534517447 |
gwascentral | rs534517447 |
openSNP | rs534517447 |
23andMe | rs534517447 |
SNPshot | rs534517447 |
SNPdbe | rs534517447 |
MSV3d | rs534517447 |
GWAS Ctlg | rs534517447 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs534517447(A;A) |
Alt | rs534517447(A;A) |
Reference | Rs534517447(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GRIK4 LOC101929208 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.120827644G>A |
CLNSRC | |
CLNACC | RCV000209911.1, |