rs886043706
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 19 |
Position | 46756125 |
Gene | FKRP |
is a | snp |
is | mentioned by |
dbSNP | rs886043706 |
dbSNP (classic) | rs886043706 |
ClinGen | rs886043706 |
ebi | rs886043706 |
HLI | rs886043706 |
Exac | rs886043706 |
Gnomad | rs886043706 |
Varsome | rs886043706 |
LitVar | rs886043706 |
Map | rs886043706 |
PheGenI | rs886043706 |
Biobank | rs886043706 |
1000 genomes | rs886043706 |
hgdp | rs886043706 |
ensembl | rs886043706 |
geneview | rs886043706 |
scholar | rs886043706 |
rs886043706 | |
pharmgkb | rs886043706 |
gwascentral | rs886043706 |
openSNP | rs886043706 |
23andMe | rs886043706 |
SNPshot | rs886043706 |
SNPdbe | rs886043706 |
MSV3d | rs886043706 |
GWAS Ctlg | rs886043706 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886043706(-;-) |
Alt | rs886043706(-;-) |
Reference | Rs886043706(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FKRP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.47259382delG |
CLNSRC | |
CLNACC | RCV000346543.1, |