rs730880632
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730880632(C;C) |
Make rs730880632(C;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 47346217 |
Gene | MYBPC3 |
is a | snp |
is | mentioned by |
dbSNP | rs730880632 |
dbSNP (classic) | rs730880632 |
ClinGen | rs730880632 |
ebi | rs730880632 |
HLI | rs730880632 |
Exac | rs730880632 |
Gnomad | rs730880632 |
Varsome | rs730880632 |
LitVar | rs730880632 |
Map | rs730880632 |
PheGenI | rs730880632 |
Biobank | rs730880632 |
1000 genomes | rs730880632 |
hgdp | rs730880632 |
ensembl | rs730880632 |
geneview | rs730880632 |
scholar | rs730880632 |
rs730880632 | |
pharmgkb | rs730880632 |
gwascentral | rs730880632 |
openSNP | rs730880632 |
23andMe | rs730880632 |
SNPshot | rs730880632 |
SNPdbe | rs730880632 |
MSV3d | rs730880632 |
GWAS Ctlg | rs730880632 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880632(C;C) |
Alt | rs730880632(C;C) |
Reference | Rs730880632(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYBPC3 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000011.9:g.47367768C>G |
CLNSRC | |
CLNACC | RCV000158329.2, |