rs772229371
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs772229371(G;T) |
Make rs772229371(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 89284741 |
Gene | ANKRD11 |
is a | snp |
is | mentioned by |
dbSNP | rs772229371 |
dbSNP (classic) | rs772229371 |
ClinGen | rs772229371 |
ebi | rs772229371 |
HLI | rs772229371 |
Exac | rs772229371 |
Gnomad | rs772229371 |
Varsome | rs772229371 |
LitVar | rs772229371 |
Map | rs772229371 |
PheGenI | rs772229371 |
Biobank | rs772229371 |
1000 genomes | rs772229371 |
hgdp | rs772229371 |
ensembl | rs772229371 |
geneview | rs772229371 |
scholar | rs772229371 |
rs772229371 | |
pharmgkb | rs772229371 |
gwascentral | rs772229371 |
openSNP | rs772229371 |
23andMe | rs772229371 |
SNPshot | rs772229371 |
SNPdbe | rs772229371 |
MSV3d | rs772229371 |
GWAS Ctlg | rs772229371 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772229371(A;A) rs772229371(T;T) |
Alt | rs772229371(A;A) rs772229371(T;T) |
Reference | Rs772229371(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANKRD11 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89351149G>A |
CLNSRC | |
CLNACC | RCV000317010.1, |