rs1060500479
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1060500479(-;-) |
Make rs1060500479(-;A) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 178581558 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs1060500479 |
dbSNP (classic) | rs1060500479 |
ClinGen | rs1060500479 |
ebi | rs1060500479 |
HLI | rs1060500479 |
Exac | rs1060500479 |
Gnomad | rs1060500479 |
Varsome | rs1060500479 |
LitVar | rs1060500479 |
Map | rs1060500479 |
PheGenI | rs1060500479 |
Biobank | rs1060500479 |
1000 genomes | rs1060500479 |
hgdp | rs1060500479 |
ensembl | rs1060500479 |
geneview | rs1060500479 |
scholar | rs1060500479 |
rs1060500479 | |
pharmgkb | rs1060500479 |
gwascentral | rs1060500479 |
openSNP | rs1060500479 |
23andMe | rs1060500479 |
SNPshot | rs1060500479 |
SNPdbe | rs1060500479 |
MSV3d | rs1060500479 |
GWAS Ctlg | rs1060500479 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060500479(-;-) |
Alt | rs1060500479(-;-) |
Reference | Rs1060500479(A;A) |
Significance | Probable-Pathogenic |
Disease | Dilated cardiomyopathy 1G |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | Dilated cardiomyopathy 1G |
Reversed | 1 |
HGVS | NC_000002.11:g.179446285delT |
CLNSRC | |
CLNACC | RCV000467745.1, |