rs876661393
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876661393(A;A) |
Make rs876661393(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 52452147 |
Gene | TNNC1 |
is a | snp |
is | mentioned by |
dbSNP | rs876661393 |
dbSNP (classic) | rs876661393 |
ClinGen | rs876661393 |
ebi | rs876661393 |
HLI | rs876661393 |
Exac | rs876661393 |
Gnomad | rs876661393 |
Varsome | rs876661393 |
LitVar | rs876661393 |
Map | rs876661393 |
PheGenI | rs876661393 |
Biobank | rs876661393 |
1000 genomes | rs876661393 |
hgdp | rs876661393 |
ensembl | rs876661393 |
geneview | rs876661393 |
scholar | rs876661393 |
rs876661393 | |
pharmgkb | rs876661393 |
gwascentral | rs876661393 |
openSNP | rs876661393 |
23andMe | rs876661393 |
SNPshot | rs876661393 |
SNPdbe | rs876661393 |
MSV3d | rs876661393 |
GWAS Ctlg | rs876661393 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661393(A;A) |
Alt | rs876661393(A;A) |
Reference | Rs876661393(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | TNNC1 |
CLNDBN | not specified not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.52486163G>T |
CLNSRC | |
CLNACC | RCV000223755.1, RCV000483835.1, |