rs730881068
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs730881068(C;T) |
Make rs730881068(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 55154821 |
Gene | TNNI3 |
is a | snp |
is | mentioned by |
dbSNP | rs730881068 |
dbSNP (classic) | rs730881068 |
ClinGen | rs730881068 |
ebi | rs730881068 |
HLI | rs730881068 |
Exac | rs730881068 |
Gnomad | rs730881068 |
Varsome | rs730881068 |
LitVar | rs730881068 |
Map | rs730881068 |
PheGenI | rs730881068 |
Biobank | rs730881068 |
1000 genomes | rs730881068 |
hgdp | rs730881068 |
ensembl | rs730881068 |
geneview | rs730881068 |
scholar | rs730881068 |
rs730881068 | |
pharmgkb | rs730881068 |
gwascentral | rs730881068 |
openSNP | rs730881068 |
23andMe | rs730881068 |
SNPshot | rs730881068 |
SNPdbe | rs730881068 |
MSV3d | rs730881068 |
GWAS Ctlg | rs730881068 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881068(G;G) rs730881068(T;T) |
Alt | rs730881068(G;G) rs730881068(T;T) |
Reference | Rs730881068(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | TNNI3 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000019.9:g.55666189G>A |
CLNSRC | |
CLNACC | RCV000159212.3, |