rs397516138
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs397516138(A;G) |
Make rs397516138(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23425775 |
Gene | MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs397516138 |
dbSNP (classic) | rs397516138 |
ClinGen | rs397516138 |
ebi | rs397516138 |
HLI | rs397516138 |
Exac | rs397516138 |
Gnomad | rs397516138 |
Varsome | rs397516138 |
LitVar | rs397516138 |
Map | rs397516138 |
PheGenI | rs397516138 |
Biobank | rs397516138 |
1000 genomes | rs397516138 |
hgdp | rs397516138 |
ensembl | rs397516138 |
geneview | rs397516138 |
scholar | rs397516138 |
rs397516138 | |
pharmgkb | rs397516138 |
gwascentral | rs397516138 |
openSNP | rs397516138 |
23andMe | rs397516138 |
SNPshot | rs397516138 |
SNPdbe | rs397516138 |
MSV3d | rs397516138 |
GWAS Ctlg | rs397516138 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397516138(G;G) |
Alt | rs397516138(G;G) |
Reference | Rs397516138(A;A) |
Significance | Probable-Pathogenic |
Disease | not specified Familial hypertrophic cardiomyopathy 1 not provided |
Variation | info |
Gene | MYH7 |
CLNDBN | not specified Familial hypertrophic cardiomyopathy 1 not provided |
Reversed | 1 |
HGVS | NC_000014.8:g.23894984T>C |
CLNSRC | |
CLNACC | RCV000035777.2, RCV000185533.2, RCV000225741.1, |