rs560020203
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs560020203(C;T) |
Make rs560020203(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 18538188 |
Gene | CACNB2, NSUN6 |
is a | snp |
is | mentioned by |
dbSNP | rs560020203 |
dbSNP (classic) | rs560020203 |
ClinGen | rs560020203 |
ebi | rs560020203 |
HLI | rs560020203 |
Exac | rs560020203 |
Gnomad | rs560020203 |
Varsome | rs560020203 |
LitVar | rs560020203 |
Map | rs560020203 |
PheGenI | rs560020203 |
Biobank | rs560020203 |
1000 genomes | rs560020203 |
hgdp | rs560020203 |
ensembl | rs560020203 |
geneview | rs560020203 |
scholar | rs560020203 |
rs560020203 | |
pharmgkb | rs560020203 |
gwascentral | rs560020203 |
openSNP | rs560020203 |
23andMe | rs560020203 |
SNPshot | rs560020203 |
SNPdbe | rs560020203 |
MSV3d | rs560020203 |
GWAS Ctlg | rs560020203 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs560020203(A;A) rs560020203(T;T) |
Alt | rs560020203(A;A) rs560020203(T;T) |
Reference | Rs560020203(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CACNB2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.18827117C>A |
CLNSRC | |
CLNACC | RCV000170867.2, |