rs549138385
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs549138385(C;T) |
Make rs549138385(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 18135747 |
Gene | MYO15A |
is a | snp |
is | mentioned by |
dbSNP | rs549138385 |
dbSNP (classic) | rs549138385 |
ClinGen | rs549138385 |
ebi | rs549138385 |
HLI | rs549138385 |
Exac | rs549138385 |
Gnomad | rs549138385 |
Varsome | rs549138385 |
LitVar | rs549138385 |
Map | rs549138385 |
PheGenI | rs549138385 |
Biobank | rs549138385 |
1000 genomes | rs549138385 |
hgdp | rs549138385 |
ensembl | rs549138385 |
geneview | rs549138385 |
scholar | rs549138385 |
rs549138385 | |
pharmgkb | rs549138385 |
gwascentral | rs549138385 |
openSNP | rs549138385 |
23andMe | rs549138385 |
SNPshot | rs549138385 |
SNPdbe | rs549138385 |
MSV3d | rs549138385 |
GWAS Ctlg | rs549138385 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs549138385(G;G) rs549138385(T;T) |
Alt | rs549138385(G;G) rs549138385(T;T) |
Reference | Rs549138385(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYO15A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.18039061C>T |
CLNSRC | |
CLNACC | RCV000483838.1, |