rs121909315
From SNPedia
Merged into | rs121908218 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909315(A;A) |
Make rs121909315(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 13303576 |
Gene | CACNA1A |
is a | snp |
is | mentioned by |
dbSNP | rs121909315 |
dbSNP (classic) | rs121909315 |
ClinGen | rs121909315 |
ebi | rs121909315 |
HLI | rs121909315 |
Exac | rs121909315 |
Gnomad | rs121909315 |
Varsome | rs121909315 |
LitVar | rs121909315 |
Map | rs121909315 |
PheGenI | rs121909315 |
Biobank | rs121909315 |
1000 genomes | rs121909315 |
hgdp | rs121909315 |
ensembl | rs121909315 |
geneview | rs121909315 |
scholar | rs121909315 |
rs121909315 | |
pharmgkb | rs121909315 |
gwascentral | rs121909315 |
openSNP | rs121909315 |
23andMe | rs121909315 |
SNPshot | rs121909315 |
SNPdbe | rs121909315 |
MSV3d | rs121909315 |
GWAS Ctlg | rs121909315 |
Status | Merged into rs121908218 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909315(A;A) |
Alt | rs121909315(A;A) |
Reference | Rs121909315(C;C) |
Significance | Untested |
Disease | |
Variation | info |
Gene | CACNA1A |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000019.9:g.13414390G>T |
CLNSRC | |
CLNACC |