rs1057520772
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1057520772(A;C) |
Make rs1057520772(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 46756844 |
Gene | FKRP |
is a | snp |
is | mentioned by |
dbSNP | rs1057520772 |
dbSNP (classic) | rs1057520772 |
ClinGen | rs1057520772 |
ebi | rs1057520772 |
HLI | rs1057520772 |
Exac | rs1057520772 |
Gnomad | rs1057520772 |
Varsome | rs1057520772 |
LitVar | rs1057520772 |
Map | rs1057520772 |
PheGenI | rs1057520772 |
Biobank | rs1057520772 |
1000 genomes | rs1057520772 |
hgdp | rs1057520772 |
ensembl | rs1057520772 |
geneview | rs1057520772 |
scholar | rs1057520772 |
rs1057520772 | |
pharmgkb | rs1057520772 |
gwascentral | rs1057520772 |
openSNP | rs1057520772 |
23andMe | rs1057520772 |
SNPshot | rs1057520772 |
SNPdbe | rs1057520772 |
MSV3d | rs1057520772 |
GWAS Ctlg | rs1057520772 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057520772(C;C) |
Alt | rs1057520772(C;C) |
Reference | Rs1057520772(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FKRP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.47260101A>C |
CLNSRC | |
CLNACC | RCV000436944.1, |