rs184280124
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs184280124(A;A) |
Make rs184280124(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 18539333 |
Gene | CACNB2, NSUN6 |
is a | snp |
is | mentioned by |
dbSNP | rs184280124 |
dbSNP (classic) | rs184280124 |
ClinGen | rs184280124 |
ebi | rs184280124 |
HLI | rs184280124 |
Exac | rs184280124 |
Gnomad | rs184280124 |
Varsome | rs184280124 |
LitVar | rs184280124 |
Map | rs184280124 |
PheGenI | rs184280124 |
Biobank | rs184280124 |
1000 genomes | rs184280124 |
hgdp | rs184280124 |
ensembl | rs184280124 |
geneview | rs184280124 |
scholar | rs184280124 |
rs184280124 | |
pharmgkb | rs184280124 |
gwascentral | rs184280124 |
openSNP | rs184280124 |
23andMe | rs184280124 |
SNPshot | rs184280124 |
SNPdbe | rs184280124 |
MSV3d | rs184280124 |
GWAS Ctlg | rs184280124 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs184280124(A;A) rs184280124(C;C) |
Alt | rs184280124(A;A) rs184280124(C;C) |
Reference | Rs184280124(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CACNB2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.18828262G>A |
CLNSRC | |
CLNACC | RCV000170872.3, |