rs112179534
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs112179534(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 47341246 |
Gene | MYBPC3 |
is a | snp |
is | mentioned by |
dbSNP | rs112179534 |
dbSNP (classic) | rs112179534 |
ClinGen | rs112179534 |
ebi | rs112179534 |
HLI | rs112179534 |
Exac | rs112179534 |
Gnomad | rs112179534 |
Varsome | rs112179534 |
LitVar | rs112179534 |
Map | rs112179534 |
PheGenI | rs112179534 |
Biobank | rs112179534 |
1000 genomes | rs112179534 |
hgdp | rs112179534 |
ensembl | rs112179534 |
geneview | rs112179534 |
scholar | rs112179534 |
rs112179534 | |
pharmgkb | rs112179534 |
gwascentral | rs112179534 |
openSNP | rs112179534 |
23andMe | rs112179534 |
SNPshot | rs112179534 |
SNPdbe | rs112179534 |
MSV3d | rs112179534 |
GWAS Ctlg | rs112179534 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs112179534(G;G) |
Alt | rs112179534(G;G) |
Reference | Rs112179534(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYBPC3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.47362797T>G |
CLNSRC | |
CLNACC | RCV000158116.1, |