rs267599036
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs267599036(C;T) |
Make rs267599036(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 178567435 |
Gene | TTN, TTN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs267599036 |
dbSNP (classic) | rs267599036 |
ClinGen | rs267599036 |
ebi | rs267599036 |
HLI | rs267599036 |
Exac | rs267599036 |
Gnomad | rs267599036 |
Varsome | rs267599036 |
LitVar | rs267599036 |
Map | rs267599036 |
PheGenI | rs267599036 |
Biobank | rs267599036 |
1000 genomes | rs267599036 |
hgdp | rs267599036 |
ensembl | rs267599036 |
geneview | rs267599036 |
scholar | rs267599036 |
rs267599036 | |
pharmgkb | rs267599036 |
gwascentral | rs267599036 |
openSNP | rs267599036 |
23andMe | rs267599036 |
SNPshot | rs267599036 |
SNPdbe | rs267599036 |
MSV3d | rs267599036 |
GWAS Ctlg | rs267599036 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267599036(A;A) rs267599036(T;T) |
Alt | rs267599036(A;A) rs267599036(T;T) |
Reference | Rs267599036(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTN TTN-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.179432162C>A |
CLNSRC | |
CLNACC | RCV000184266.2, |