rs150001589
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs150001589(A;A) |
Make rs150001589(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 68214309 |
Gene | CLN6 |
is a | snp |
is | mentioned by |
dbSNP | rs150001589 |
dbSNP (classic) | rs150001589 |
ClinGen | rs150001589 |
ebi | rs150001589 |
HLI | rs150001589 |
Exac | rs150001589 |
Gnomad | rs150001589 |
Varsome | rs150001589 |
LitVar | rs150001589 |
Map | rs150001589 |
PheGenI | rs150001589 |
Biobank | rs150001589 |
1000 genomes | rs150001589 |
hgdp | rs150001589 |
ensembl | rs150001589 |
geneview | rs150001589 |
scholar | rs150001589 |
rs150001589 | |
pharmgkb | rs150001589 |
gwascentral | rs150001589 |
openSNP | rs150001589 |
23andMe | rs150001589 |
SNPshot | rs150001589 |
SNPdbe | rs150001589 |
MSV3d | rs150001589 |
GWAS Ctlg | rs150001589 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs150001589(A;A) |
Alt | rs150001589(A;A) |
Reference | Rs150001589(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | CLN6 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.68506647G>A |
CLNSRC | |
CLNACC | RCV000187115.3, |