rs2050656
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs2050656(A;A) |
Make rs2050656(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 237347614 |
Gene | RYR2 |
is a | snp |
is | mentioned by |
dbSNP | rs2050656 |
dbSNP (classic) | rs2050656 |
ClinGen | rs2050656 |
ebi | rs2050656 |
HLI | rs2050656 |
Exac | rs2050656 |
Gnomad | rs2050656 |
Varsome | rs2050656 |
LitVar | rs2050656 |
Map | rs2050656 |
PheGenI | rs2050656 |
Biobank | rs2050656 |
1000 genomes | rs2050656 |
hgdp | rs2050656 |
ensembl | rs2050656 |
geneview | rs2050656 |
scholar | rs2050656 |
rs2050656 | |
pharmgkb | rs2050656 |
gwascentral | rs2050656 |
openSNP | rs2050656 |
23andMe | rs2050656 |
SNPshot | rs2050656 |
SNPdbe | rs2050656 |
MSV3d | rs2050656 |
GWAS Ctlg | rs2050656 |
GMAF | 0.1837 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.[PMID 19626040]