rs761848111
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs761848111(A;A) |
Make rs761848111(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 89282980 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs761848111 |
dbSNP (classic) | rs761848111 |
ClinGen | rs761848111 |
ebi | rs761848111 |
HLI | rs761848111 |
Exac | rs761848111 |
Gnomad | rs761848111 |
Varsome | rs761848111 |
LitVar | rs761848111 |
Map | rs761848111 |
PheGenI | rs761848111 |
Biobank | rs761848111 |
1000 genomes | rs761848111 |
hgdp | rs761848111 |
ensembl | rs761848111 |
geneview | rs761848111 |
scholar | rs761848111 |
rs761848111 | |
pharmgkb | rs761848111 |
gwascentral | rs761848111 |
openSNP | rs761848111 |
23andMe | rs761848111 |
SNPshot | rs761848111 |
SNPdbe | rs761848111 |
MSV3d | rs761848111 |
GWAS Ctlg | rs761848111 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761848111(A;A) |
Alt | rs761848111(A;A) |
Reference | Rs761848111(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANKRD11 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89349388G>A |
CLNSRC | |
CLNACC | RCV000266509.1, |