rs746852311
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs746852311(A;A) |
Make rs746852311(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 89288598 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs746852311 |
dbSNP (classic) | rs746852311 |
ClinGen | rs746852311 |
ebi | rs746852311 |
HLI | rs746852311 |
Exac | rs746852311 |
Gnomad | rs746852311 |
Varsome | rs746852311 |
LitVar | rs746852311 |
Map | rs746852311 |
PheGenI | rs746852311 |
Biobank | rs746852311 |
1000 genomes | rs746852311 |
hgdp | rs746852311 |
ensembl | rs746852311 |
geneview | rs746852311 |
scholar | rs746852311 |
rs746852311 | |
pharmgkb | rs746852311 |
gwascentral | rs746852311 |
openSNP | rs746852311 |
23andMe | rs746852311 |
SNPshot | rs746852311 |
SNPdbe | rs746852311 |
MSV3d | rs746852311 |
GWAS Ctlg | rs746852311 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs746852311(A;A) |
Alt | rs746852311(A;A) |
Reference | Rs746852311(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANKRD11 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89355006G>A |
CLNSRC | |
CLNACC | RCV000413362.1, |