rs730880887
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GAG;GAG) | 0 | common in clinvar |
Make rs730880887(-;-) |
Make rs730880887(-;GAG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23424883 |
Gene | MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs730880887 |
dbSNP (classic) | rs730880887 |
ClinGen | rs730880887 |
ebi | rs730880887 |
HLI | rs730880887 |
Exac | rs730880887 |
Gnomad | rs730880887 |
Varsome | rs730880887 |
LitVar | rs730880887 |
Map | rs730880887 |
PheGenI | rs730880887 |
Biobank | rs730880887 |
1000 genomes | rs730880887 |
hgdp | rs730880887 |
ensembl | rs730880887 |
geneview | rs730880887 |
scholar | rs730880887 |
rs730880887 | |
pharmgkb | rs730880887 |
gwascentral | rs730880887 |
openSNP | rs730880887 |
23andMe | rs730880887 |
SNPshot | rs730880887 |
SNPdbe | rs730880887 |
MSV3d | rs730880887 |
GWAS Ctlg | rs730880887 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880887(-;-) |
Alt | rs730880887(-;-) |
Reference | Rs730880887(GAG;GAG) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYH7 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000014.8:g.23894092_23894094delCTC |
CLNSRC | |
CLNACC | RCV000158828.1, |