rs869312699
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CTGGCGCAGGAGGCC;CTGGCGCAGGAGGCC) | 0 | common in clinvar |
Make rs869312699(CTGGCGCAGGAGGCC;GCT) |
Make rs869312699(GCT;GCT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 120986102 |
Gene | GRIK4 |
is a | snp |
is | mentioned by |
dbSNP | rs869312699 |
dbSNP (classic) | rs869312699 |
ClinGen | rs869312699 |
ebi | rs869312699 |
HLI | rs869312699 |
Exac | rs869312699 |
Gnomad | rs869312699 |
Varsome | rs869312699 |
LitVar | rs869312699 |
Map | rs869312699 |
PheGenI | rs869312699 |
Biobank | rs869312699 |
1000 genomes | rs869312699 |
hgdp | rs869312699 |
ensembl | rs869312699 |
geneview | rs869312699 |
scholar | rs869312699 |
rs869312699 | |
pharmgkb | rs869312699 |
gwascentral | rs869312699 |
openSNP | rs869312699 |
23andMe | rs869312699 |
SNPshot | rs869312699 |
SNPdbe | rs869312699 |
MSV3d | rs869312699 |
GWAS Ctlg | rs869312699 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869312699(GCT;GCT) |
Alt | rs869312699(GCT;GCT) |
Reference | Rs869312699(CTGGCGCAGGAGGCC;CTGGCGCAGGAGGCC) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GRIK4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.120856811_120856825delCTGGCGCAGGAGGCCinsGCT |
CLNSRC | |
CLNACC | RCV000209841.1, |