rs774528745
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs774528745(C;T) |
Make rs774528745(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 222221368 |
Gene | LOC105373901, LOC107985991, PAX3 |
is a | snp |
is | mentioned by |
dbSNP | rs774528745 |
dbSNP (classic) | rs774528745 |
ClinGen | rs774528745 |
ebi | rs774528745 |
HLI | rs774528745 |
Exac | rs774528745 |
Gnomad | rs774528745 |
Varsome | rs774528745 |
LitVar | rs774528745 |
Map | rs774528745 |
PheGenI | rs774528745 |
Biobank | rs774528745 |
1000 genomes | rs774528745 |
hgdp | rs774528745 |
ensembl | rs774528745 |
geneview | rs774528745 |
scholar | rs774528745 |
rs774528745 | |
pharmgkb | rs774528745 |
gwascentral | rs774528745 |
openSNP | rs774528745 |
23andMe | rs774528745 |
SNPshot | rs774528745 |
SNPdbe | rs774528745 |
MSV3d | rs774528745 |
GWAS Ctlg | rs774528745 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs774528745(T;T) |
Alt | rs774528745(T;T) |
Reference | Rs774528745(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PAX3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.223086087C>T |
CLNSRC | |
CLNACC | RCV000372931.1, |