rs727504352
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs727504352(C;T) |
Make rs727504352(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23418349 |
Gene | MIR208B, MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs727504352 |
dbSNP (classic) | rs727504352 |
ClinGen | rs727504352 |
ebi | rs727504352 |
HLI | rs727504352 |
Exac | rs727504352 |
Gnomad | rs727504352 |
Varsome | rs727504352 |
LitVar | rs727504352 |
Map | rs727504352 |
PheGenI | rs727504352 |
Biobank | rs727504352 |
1000 genomes | rs727504352 |
hgdp | rs727504352 |
ensembl | rs727504352 |
geneview | rs727504352 |
scholar | rs727504352 |
rs727504352 | |
pharmgkb | rs727504352 |
gwascentral | rs727504352 |
openSNP | rs727504352 |
23andMe | rs727504352 |
SNPshot | rs727504352 |
SNPdbe | rs727504352 |
MSV3d | rs727504352 |
GWAS Ctlg | rs727504352 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727504352(A;A) rs727504352(T;T) |
Alt | rs727504352(A;A) rs727504352(T;T) |
Reference | Rs727504352(C;C) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | MYH7 MIR208B |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000014.8:g.23887558G>A |
CLNSRC | |
CLNACC | RCV000154475.2, |