rs150008205
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs150008205(C;T) |
Make rs150008205(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 201362019 |
Gene | TNNT2 |
is a | snp |
is | mentioned by |
dbSNP | rs150008205 |
dbSNP (classic) | rs150008205 |
ClinGen | rs150008205 |
ebi | rs150008205 |
HLI | rs150008205 |
Exac | rs150008205 |
Gnomad | rs150008205 |
Varsome | rs150008205 |
LitVar | rs150008205 |
Map | rs150008205 |
PheGenI | rs150008205 |
Biobank | rs150008205 |
1000 genomes | rs150008205 |
hgdp | rs150008205 |
ensembl | rs150008205 |
geneview | rs150008205 |
scholar | rs150008205 |
rs150008205 | |
pharmgkb | rs150008205 |
gwascentral | rs150008205 |
openSNP | rs150008205 |
23andMe | rs150008205 |
SNPshot | rs150008205 |
SNPdbe | rs150008205 |
MSV3d | rs150008205 |
GWAS Ctlg | rs150008205 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs150008205(T;T) |
Alt | rs150008205(T;T) |
Reference | Rs150008205(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TNNT2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.201331147C>T |
CLNSRC | |
CLNACC | RCV000159306.1, |