rs540263945
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs540263945(C;G) |
Make rs540263945(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23419587 |
Gene | MIR208B, MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs540263945 |
dbSNP (classic) | rs540263945 |
ClinGen | rs540263945 |
ebi | rs540263945 |
HLI | rs540263945 |
Exac | rs540263945 |
Gnomad | rs540263945 |
Varsome | rs540263945 |
LitVar | rs540263945 |
Map | rs540263945 |
PheGenI | rs540263945 |
Biobank | rs540263945 |
1000 genomes | rs540263945 |
hgdp | rs540263945 |
ensembl | rs540263945 |
geneview | rs540263945 |
scholar | rs540263945 |
rs540263945 | |
pharmgkb | rs540263945 |
gwascentral | rs540263945 |
openSNP | rs540263945 |
23andMe | rs540263945 |
SNPshot | rs540263945 |
SNPdbe | rs540263945 |
MSV3d | rs540263945 |
GWAS Ctlg | rs540263945 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs540263945(G;G) rs540263945(T;T) |
Alt | rs540263945(G;G) rs540263945(T;T) |
Reference | Rs540263945(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYH7 MIR208B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.23888796C>G |
CLNSRC | |
CLNACC | RCV000158619.1, |