rs730880954
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730880954(A;A) |
Make rs730880954(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 46860799 |
Gene | MYL3 |
is a | snp |
is | mentioned by |
dbSNP | rs730880954 |
dbSNP (classic) | rs730880954 |
ClinGen | rs730880954 |
ebi | rs730880954 |
HLI | rs730880954 |
Exac | rs730880954 |
Gnomad | rs730880954 |
Varsome | rs730880954 |
LitVar | rs730880954 |
Map | rs730880954 |
PheGenI | rs730880954 |
Biobank | rs730880954 |
1000 genomes | rs730880954 |
hgdp | rs730880954 |
ensembl | rs730880954 |
geneview | rs730880954 |
scholar | rs730880954 |
rs730880954 | |
pharmgkb | rs730880954 |
gwascentral | rs730880954 |
openSNP | rs730880954 |
23andMe | rs730880954 |
SNPshot | rs730880954 |
SNPdbe | rs730880954 |
MSV3d | rs730880954 |
GWAS Ctlg | rs730880954 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880954(A;A) |
Alt | rs730880954(A;A) |
Reference | Rs730880954(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | MYL3 |
CLNDBN | not provided not specified |
Reversed | 1 |
HGVS | NC_000003.11:g.46902289C>T |
CLNSRC | |
CLNACC | RCV000158939.2, RCV000214205.1, |