rs886041841
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CAG;CAG) | 0 | common in clinvar |
Chromosome | 11 |
Position | 47441668 |
Gene | RAPSN |
is a | snp |
is | mentioned by |
dbSNP | rs886041841 |
dbSNP (classic) | rs886041841 |
ClinGen | rs886041841 |
ebi | rs886041841 |
HLI | rs886041841 |
Exac | rs886041841 |
Gnomad | rs886041841 |
Varsome | rs886041841 |
LitVar | rs886041841 |
Map | rs886041841 |
PheGenI | rs886041841 |
Biobank | rs886041841 |
1000 genomes | rs886041841 |
hgdp | rs886041841 |
ensembl | rs886041841 |
geneview | rs886041841 |
scholar | rs886041841 |
rs886041841 | |
pharmgkb | rs886041841 |
gwascentral | rs886041841 |
openSNP | rs886041841 |
23andMe | rs886041841 |
SNPshot | rs886041841 |
SNPdbe | rs886041841 |
MSV3d | rs886041841 |
GWAS Ctlg | rs886041841 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041841(TAA;TAA) |
Alt | rs886041841(TAA;TAA) |
Reference | Rs886041841(CAG;CAG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RAPSN |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000011.9:g.47463220_47463222delCTGinsTTA |
CLNSRC | |
CLNACC | RCV000348754.1, |