rs766840243
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs766840243(A;A) |
Make rs766840243(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178563892 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs766840243 |
dbSNP (classic) | rs766840243 |
ClinGen | rs766840243 |
ebi | rs766840243 |
HLI | rs766840243 |
Exac | rs766840243 |
Gnomad | rs766840243 |
Varsome | rs766840243 |
LitVar | rs766840243 |
Map | rs766840243 |
PheGenI | rs766840243 |
Biobank | rs766840243 |
1000 genomes | rs766840243 |
hgdp | rs766840243 |
ensembl | rs766840243 |
geneview | rs766840243 |
scholar | rs766840243 |
rs766840243 | |
pharmgkb | rs766840243 |
gwascentral | rs766840243 |
openSNP | rs766840243 |
23andMe | rs766840243 |
SNPshot | rs766840243 |
SNPdbe | rs766840243 |
MSV3d | rs766840243 |
GWAS Ctlg | rs766840243 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs766840243(A;A) rs766840243(C;C) |
Alt | rs766840243(A;A) rs766840243(C;C) |
Reference | Rs766840243(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179428619G>A |
CLNSRC | |
CLNACC | RCV000184271.3, |