rs753444140
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs753444140(A;A) |
Make rs753444140(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 23402497 |
Gene | MYH6 |
is a | snp |
is | mentioned by |
dbSNP | rs753444140 |
dbSNP (classic) | rs753444140 |
ClinGen | rs753444140 |
ebi | rs753444140 |
HLI | rs753444140 |
Exac | rs753444140 |
Gnomad | rs753444140 |
Varsome | rs753444140 |
LitVar | rs753444140 |
Map | rs753444140 |
PheGenI | rs753444140 |
Biobank | rs753444140 |
1000 genomes | rs753444140 |
hgdp | rs753444140 |
ensembl | rs753444140 |
geneview | rs753444140 |
scholar | rs753444140 |
rs753444140 | |
pharmgkb | rs753444140 |
gwascentral | rs753444140 |
openSNP | rs753444140 |
23andMe | rs753444140 |
SNPshot | rs753444140 |
SNPdbe | rs753444140 |
MSV3d | rs753444140 |
GWAS Ctlg | rs753444140 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs753444140(A;A) |
Alt | rs753444140(A;A) |
Reference | Rs753444140(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYH6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.23871706G>A |
CLNSRC | |
CLNACC | RCV000485434.1, |