rs121908211
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121908211(A;A) |
Make rs121908211(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 13371744 |
Gene | CACNA1A |
is a | snp |
is | mentioned by |
dbSNP | rs121908211 |
dbSNP (classic) | rs121908211 |
ClinGen | rs121908211 |
ebi | rs121908211 |
HLI | rs121908211 |
Exac | rs121908211 |
Gnomad | rs121908211 |
Varsome | rs121908211 |
LitVar | rs121908211 |
Map | rs121908211 |
PheGenI | rs121908211 |
Biobank | rs121908211 |
1000 genomes | rs121908211 |
hgdp | rs121908211 |
ensembl | rs121908211 |
geneview | rs121908211 |
scholar | rs121908211 |
rs121908211 | |
pharmgkb | rs121908211 |
gwascentral | rs121908211 |
openSNP | rs121908211 |
23andMe | rs121908211 |
SNPshot | rs121908211 |
SNPdbe | rs121908211 |
MSV3d | rs121908211 |
GWAS Ctlg | rs121908211 |
Merged from | Rs121909310 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908211(A;A) |
Alt | rs121908211(A;A) |
Reference | Rs121908211(G;G) |
Significance | Pathogenic |
Disease | Familial hemiplegic migraine type 1 |
Variation | info |
Gene | CACNA1A |
CLNDBN | Familial hemiplegic migraine type 1 |
Reversed | 1 |
HGVS | NC_000019.9:g.13482558C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (variants) |
CLNACC | RCV000009008.4, |