rs745998610
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs745998610(A;A) |
Make rs745998610(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 201077912 |
Gene | CACNA1S |
is a | snp |
is | mentioned by |
dbSNP | rs745998610 |
dbSNP (classic) | rs745998610 |
ClinGen | rs745998610 |
ebi | rs745998610 |
HLI | rs745998610 |
Exac | rs745998610 |
Gnomad | rs745998610 |
Varsome | rs745998610 |
LitVar | rs745998610 |
Map | rs745998610 |
PheGenI | rs745998610 |
Biobank | rs745998610 |
1000 genomes | rs745998610 |
hgdp | rs745998610 |
ensembl | rs745998610 |
geneview | rs745998610 |
scholar | rs745998610 |
rs745998610 | |
pharmgkb | rs745998610 |
gwascentral | rs745998610 |
openSNP | rs745998610 |
23andMe | rs745998610 |
SNPshot | rs745998610 |
SNPdbe | rs745998610 |
MSV3d | rs745998610 |
GWAS Ctlg | rs745998610 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745998610(A;A) |
Alt | rs745998610(A;A) |
Reference | Rs745998610(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CACNA1S |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.201047040C>A |
CLNSRC | |
CLNACC | RCV000181042.1, |