rs45501500
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45501500(A;A) |
Make rs45501500(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 201363390 |
Gene | TNNT2 |
is a | snp |
is | mentioned by |
dbSNP | rs45501500 |
dbSNP (classic) | rs45501500 |
ClinGen | rs45501500 |
ebi | rs45501500 |
HLI | rs45501500 |
Exac | rs45501500 |
Gnomad | rs45501500 |
Varsome | rs45501500 |
LitVar | rs45501500 |
Map | rs45501500 |
PheGenI | rs45501500 |
Biobank | rs45501500 |
1000 genomes | rs45501500 |
hgdp | rs45501500 |
ensembl | rs45501500 |
geneview | rs45501500 |
scholar | rs45501500 |
rs45501500 | |
pharmgkb | rs45501500 |
gwascentral | rs45501500 |
openSNP | rs45501500 |
23andMe | rs45501500 |
SNPshot | rs45501500 |
SNPdbe | rs45501500 |
MSV3d | rs45501500 |
GWAS Ctlg | rs45501500 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45501500(A;A) |
Alt | rs45501500(A;A) |
Reference | Rs45501500(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | TNNT2 |
CLNDBN | not specified not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.201332518C>T |
CLNSRC | |
CLNACC | RCV000036595.3, RCV000225721.1, |