rs369751362
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs369751362(C;T) |
Make rs369751362(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 15720895 |
Gene | MYH11, NDE1 |
is a | snp |
is | mentioned by |
dbSNP | rs369751362 |
dbSNP (classic) | rs369751362 |
ClinGen | rs369751362 |
ebi | rs369751362 |
HLI | rs369751362 |
Exac | rs369751362 |
Gnomad | rs369751362 |
Varsome | rs369751362 |
LitVar | rs369751362 |
Map | rs369751362 |
PheGenI | rs369751362 |
Biobank | rs369751362 |
1000 genomes | rs369751362 |
hgdp | rs369751362 |
ensembl | rs369751362 |
geneview | rs369751362 |
scholar | rs369751362 |
rs369751362 | |
pharmgkb | rs369751362 |
gwascentral | rs369751362 |
openSNP | rs369751362 |
23andMe | rs369751362 |
SNPshot | rs369751362 |
SNPdbe | rs369751362 |
MSV3d | rs369751362 |
GWAS Ctlg | rs369751362 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369751362(T;T) |
Alt | rs369751362(T;T) |
Reference | Rs369751362(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | NDE1 MYH11 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000016.9:g.15814752C>T |
CLNSRC | |
CLNACC | RCV000182523.3, |