rs397516341
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs397516341(A;G) |
Make rs397516341(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 55157589 |
Gene | LOC101930593, TNNI3 |
is a | snp |
is | mentioned by |
dbSNP | rs397516341 |
dbSNP (classic) | rs397516341 |
ClinGen | rs397516341 |
ebi | rs397516341 |
HLI | rs397516341 |
Exac | rs397516341 |
Gnomad | rs397516341 |
Varsome | rs397516341 |
LitVar | rs397516341 |
Map | rs397516341 |
PheGenI | rs397516341 |
Biobank | rs397516341 |
1000 genomes | rs397516341 |
hgdp | rs397516341 |
ensembl | rs397516341 |
geneview | rs397516341 |
scholar | rs397516341 |
rs397516341 | |
pharmgkb | rs397516341 |
gwascentral | rs397516341 |
openSNP | rs397516341 |
23andMe | rs397516341 |
SNPshot | rs397516341 |
SNPdbe | rs397516341 |
MSV3d | rs397516341 |
GWAS Ctlg | rs397516341 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397516341(G;G) |
Alt | rs397516341(G;G) |
Reference | Rs397516341(A;A) |
Significance | Probable-Pathogenic |
Disease | Primary familial hypertrophic cardiomyopathy |
Variation | info |
Gene | TNNI3 |
CLNDBN | Primary familial hypertrophic cardiomyopathy |
Reversed | 1 |
HGVS | NC_000019.9:g.55668957T>C |
CLNSRC | ClinVar |
CLNACC | RCV000036273.2, |