rs779093807
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs779093807(A;A) |
Make rs779093807(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 18166449 |
Gene | MYO15A |
is a | snp |
is | mentioned by |
dbSNP | rs779093807 |
dbSNP (classic) | rs779093807 |
ClinGen | rs779093807 |
ebi | rs779093807 |
HLI | rs779093807 |
Exac | rs779093807 |
Gnomad | rs779093807 |
Varsome | rs779093807 |
LitVar | rs779093807 |
Map | rs779093807 |
PheGenI | rs779093807 |
Biobank | rs779093807 |
1000 genomes | rs779093807 |
hgdp | rs779093807 |
ensembl | rs779093807 |
geneview | rs779093807 |
scholar | rs779093807 |
rs779093807 | |
pharmgkb | rs779093807 |
gwascentral | rs779093807 |
openSNP | rs779093807 |
23andMe | rs779093807 |
SNPshot | rs779093807 |
SNPdbe | rs779093807 |
MSV3d | rs779093807 |
GWAS Ctlg | rs779093807 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs779093807(A;A) rs779093807(T;T) |
Alt | rs779093807(A;A) rs779093807(T;T) |
Reference | Rs779093807(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYO15A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.18069763G>A |
CLNSRC | |
CLNACC | RCV000433268.1, |