rs397516086
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs397516086(A;A) |
Make rs397516086(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 47346303 |
Gene | MYBPC3 |
is a | snp |
is | mentioned by |
dbSNP | rs397516086 |
dbSNP (classic) | rs397516086 |
ClinGen | rs397516086 |
ebi | rs397516086 |
HLI | rs397516086 |
Exac | rs397516086 |
Gnomad | rs397516086 |
Varsome | rs397516086 |
LitVar | rs397516086 |
Map | rs397516086 |
PheGenI | rs397516086 |
Biobank | rs397516086 |
1000 genomes | rs397516086 |
hgdp | rs397516086 |
ensembl | rs397516086 |
geneview | rs397516086 |
scholar | rs397516086 |
rs397516086 | |
pharmgkb | rs397516086 |
gwascentral | rs397516086 |
openSNP | rs397516086 |
23andMe | rs397516086 |
SNPshot | rs397516086 |
SNPdbe | rs397516086 |
MSV3d | rs397516086 |
GWAS Ctlg | rs397516086 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397516086(A;A) |
Alt | rs397516086(A;A) |
Reference | Rs397516086(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | MYBPC3 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000011.9:g.47367854C>T |
CLNSRC | |
CLNACC | RCV000035691.3, |