rs45520836
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45520836(A;A) |
Make rs45520836(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 14 |
Position | 23414074 |
Gene | MHRT, MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs45520836 |
dbSNP (classic) | rs45520836 |
ClinGen | rs45520836 |
ebi | rs45520836 |
HLI | rs45520836 |
Exac | rs45520836 |
Gnomad | rs45520836 |
Varsome | rs45520836 |
LitVar | rs45520836 |
Map | rs45520836 |
PheGenI | rs45520836 |
Biobank | rs45520836 |
1000 genomes | rs45520836 |
hgdp | rs45520836 |
ensembl | rs45520836 |
geneview | rs45520836 |
scholar | rs45520836 |
rs45520836 | |
pharmgkb | rs45520836 |
gwascentral | rs45520836 |
openSNP | rs45520836 |
23andMe | rs45520836 |
SNPshot | rs45520836 |
SNPdbe | rs45520836 |
MSV3d | rs45520836 |
GWAS Ctlg | rs45520836 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45520836(A;A) |
Alt | rs45520836(A;A) |
Reference | Rs45520836(G;G) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | MYH7 MHRT |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000014.8:g.23883283C>T |
CLNSRC | ClinVar |
CLNACC | RCV000035971.3, |