rs762381137
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs762381137(A;G) |
Make rs762381137(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 115717869 |
Gene | CASQ2 |
is a | snp |
is | mentioned by |
dbSNP | rs762381137 |
dbSNP (classic) | rs762381137 |
ClinGen | rs762381137 |
ebi | rs762381137 |
HLI | rs762381137 |
Exac | rs762381137 |
Gnomad | rs762381137 |
Varsome | rs762381137 |
LitVar | rs762381137 |
Map | rs762381137 |
PheGenI | rs762381137 |
Biobank | rs762381137 |
1000 genomes | rs762381137 |
hgdp | rs762381137 |
ensembl | rs762381137 |
geneview | rs762381137 |
scholar | rs762381137 |
rs762381137 | |
pharmgkb | rs762381137 |
gwascentral | rs762381137 |
openSNP | rs762381137 |
23andMe | rs762381137 |
SNPshot | rs762381137 |
SNPdbe | rs762381137 |
MSV3d | rs762381137 |
GWAS Ctlg | rs762381137 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs762381137(G;G) |
Alt | rs762381137(G;G) |
Reference | Rs762381137(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CASQ2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.116260490A>G |
CLNSRC | |
CLNACC | RCV000170892.2, |