rs397516348
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397516348(A;A) |
Make rs397516348(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 55154151 |
Gene | TNNI3 |
is a | snp |
is | mentioned by |
dbSNP | rs397516348 |
dbSNP (classic) | rs397516348 |
ClinGen | rs397516348 |
ebi | rs397516348 |
HLI | rs397516348 |
Exac | rs397516348 |
Gnomad | rs397516348 |
Varsome | rs397516348 |
LitVar | rs397516348 |
Map | rs397516348 |
PheGenI | rs397516348 |
Biobank | rs397516348 |
1000 genomes | rs397516348 |
hgdp | rs397516348 |
ensembl | rs397516348 |
geneview | rs397516348 |
scholar | rs397516348 |
rs397516348 | |
pharmgkb | rs397516348 |
gwascentral | rs397516348 |
openSNP | rs397516348 |
23andMe | rs397516348 |
SNPshot | rs397516348 |
SNPdbe | rs397516348 |
MSV3d | rs397516348 |
GWAS Ctlg | rs397516348 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397516348(A;A) |
Alt | rs397516348(A;A) |
Reference | Rs397516348(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | TNNI3 |
CLNDBN | not specified not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.55665519G>T |
CLNSRC | |
CLNACC | RCV000036291.2, RCV000159221.2, |