rs751502842
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs751502842(G;T) |
Make rs751502842(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178612442 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs751502842 |
dbSNP (classic) | rs751502842 |
ClinGen | rs751502842 |
ebi | rs751502842 |
HLI | rs751502842 |
Exac | rs751502842 |
Gnomad | rs751502842 |
Varsome | rs751502842 |
LitVar | rs751502842 |
Map | rs751502842 |
PheGenI | rs751502842 |
Biobank | rs751502842 |
1000 genomes | rs751502842 |
hgdp | rs751502842 |
ensembl | rs751502842 |
geneview | rs751502842 |
scholar | rs751502842 |
rs751502842 | |
pharmgkb | rs751502842 |
gwascentral | rs751502842 |
openSNP | rs751502842 |
23andMe | rs751502842 |
SNPshot | rs751502842 |
SNPdbe | rs751502842 |
MSV3d | rs751502842 |
GWAS Ctlg | rs751502842 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs751502842(A;A) rs751502842(T;T) |
Alt | rs751502842(A;A) rs751502842(T;T) |
Reference | Rs751502842(G;G) |
Significance | Pathogenic |
Disease | not provided Cardiovascular phenotype not specified |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided Cardiovascular phenotype not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.179477169G>A; NC_000002.11:g.179477169G>T |
CLNSRC | |
CLNACC | RCV000184224.2, RCV000245414.1, RCV000436430.1, |